NUTRI-GRADE REQUIREMENTS FOR BEVERAGES |
184A.—(1) In these Regulations, “Nutri-Grade beverage” means any beverage (including any powder or concentrate meant to be reconstituted or diluted with fluids before consumption as a beverage) other than the following: (a) | a beverage that contains more than 0.5% (v/v) alcohol at 20ºC; | (b) | [Deleted by S 451/2023 wef 30/12/2023] | (c) | [Deleted by S 451/2023 wef 30/12/2023] | (d) | a beverage mentioned in paragraph (2). |
(2) A Nutri-Grade beverage does not include any special purpose food —(a) | for a special medical purpose and that is labelled as being for use under medical supervision; | (b) | supplied solely to hospitals, hospices and other residential care facilities like nursing homes for the purpose of providing services to patients in those facilities; | (c) | that is infant formula; | (d) | that is follow-up formula, that is, food intended for use as a liquid part of the weaning for an infant 6 months or older or young children; | (e) | that is formula food for use in a weight control diet, that is, formula food presented as a replacement for a person’s total daily diet; | (f) | that is diabetic food; or | (g) | for a person who requires a specific intake of sugar (including but not limited to sucrose) or saturated fat in the person’s diet as a result of a disease, disorder or other condition. |
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(3) In this regulation, “special medical purpose”, in relation to special purpose food, means special purpose food specially processed or formulated and presented for use under medical supervision for the dietary management of a patient —(a) | who has —(i) | limited or impaired capacity to take, digest, absorb or metabolise ordinary food or certain nutrients contained in ordinary food; or | (ii) | any other special medically-determined nutrient requirement; and |
| (b) | whose dietary management cannot be achieved only by modifying that patient’s normal diet or by other special purpose food or both. [S 993/2021 wef 30/12/2022] |
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Nutri-Grade grading system |
184B.—(1) The following persons must ensure that the following Nutri-Grade beverages are graded “A”, “B”, “C” or “D” according to the grading system specified in the Sixteenth Schedule: (a) | a Nutri-Grade beverage that is not freshly prepared and is intended for sale in a specified setting —(i) | if the Nutri-Grade beverage is manufactured in Singapore — its manufacturer; | (ii) | if the Nutri-Grade beverage is imported — its local importer; and | (iii) | in any other case — its distributor; [S 451/2023 wef 30/12/2023] |
| (b) | a Nutri-Grade beverage that is freshly prepared and is intended for sale in a specified setting —(i) | if the Nutri-Grade beverage is prepared by hand at any place or premises — its seller; and | (ii) | if the Nutri-Grade beverage is sold from an automated beverage dispenser for customisable beverages — the person who calibrates the automated beverage dispenser to be able to dispense beverages according to inputs given by a prospective consumer of the beverage. [S 451/2023 wef 30/12/2023] |
| (c) | [Deleted by S 451/2023 wef 30/12/2023] [S 451/2023 wef 30/12/2023] |
(2) In these Regulations, a reference to the grade of a Nutri-Grade beverage refers to its grade according to that grading system. [S 993/2021 wef 30/12/2022] |
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Nutrition information of Nutri-Grade beverages |
184C.—(1) A person required by regulation 184B(1) to ensure a prepacked Nutri-Grade beverage that is not freshly prepared and is intended for sale in a specified setting, is graded must ensure the package of the Nutri-Grade beverage is labelled with a nutrition information panel that —(a) | is in the form specified in the Twelfth Schedule or in any other similar form that may be acceptable to the Director-General; | (b) | specifies the energy value, the amounts of protein, carbohydrate and fat in the Nutri-Grade beverage; | (c) | unless the Nutri-Grade beverage contains no carbohydrates, specifies the amount of total sugar according to either or both of the following proportions: (i) | in grams per 100 ml of the Nutri-Grade beverage; | (ii) | if the number of servings per package and serving size are stated, in grams per serving of the Nutri‑Grade beverage; |
| (d) | unless the Nutri-Grade beverage contains no fat, specifies the amount of saturated fat according to either or both of the proportions mentioned in sub‑paragraph (c)(i) and (ii); and | (e) | where the nutrition information panel specifies the amount of lactose or galactose, specifies the amount according to either or both of the proportions mentioned in sub‑paragraph (c)(i) and (ii). [S 451/2023 wef 30/12/2023] |
(2) Where the prepacked Nutri-Grade beverage mentioned in paragraph (1) is a powder or concentrate meant to be reconstituted or diluted with fluids before consumption as a beverage, the person must (in addition to complying with that paragraph) ensure — (a) | the nutrition information panel —(i) | specifies the information that is required under that paragraph on the basis that the Nutri-Grade beverage is prepared according to the manufacturer’s instructions on how to prepare the Nutri-Grade beverage; and | (ii) | if that information is expressed as grams per 100 ml of the Nutri-Grade beverage, states that the information is on the basis that the Nutri-Grade beverage is prepared according to those instructions; and |
| (b) | the package of the Nutri-Grade beverage is labelled with those instructions. |
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(3) For the purpose of paragraph (1), where more than one unit of prepacked Nutri-Grade beverage is packaged for sale as a single item, the requirement to ensure the package is labelled under that paragraph may be satisfied by —(a) | ensuring the package of each unit of the prepacked Nutri-Grade beverage is labelled; or | (b) | ensuring the package to be sold as a single item is labelled in respect of each type of Nutri-Grade beverage within the package and the package includes a statement that each unit in the package must not be sold separately or a statement to the like effect. |
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(4) If —(a) | a person is required by regulation 184B(1) to ensure a Nutri-Grade beverage intended for sale in a specified setting is graded; and | (b) | the Nutri-Grade beverage is freshly prepared or sold from an automated beverage dispenser for non-customisable beverages, |
then the person must ensure that a nutrition information panel for the Nutri-Grade beverage that satisfies the requirements in paragraph (1) is made available (in any manner described in paragraph (5)) to any person who wishes to view the nutrition information panel. |
[S 451/2023 wef 30/12/2023] |
(4A) For the purpose of paragraph (4) —(a) | where there is a preparation of the freshly prepared Nutri-Grade beverage offered to a prospective consumer who does not customise the amount of any ingredient in the Nutri-Grade beverage (called the default preparation) — the nutrition information panel must be based on the default preparation; or | (b) | where the freshly prepared Nutri-Grade beverage does not have a default preparation and a prospective customer must customise the amount of any one or more ingredients in the Nutri-Grade beverage, the nutrition information panel must be based on —(i) | the customised preparation of the Nutri-Grade beverage with the poorest grade from amongst all possible customised preparations of the Nutri-Grade beverage offered to prospective consumers; and | (ii) | if there is more than one such customised preparation with that grade, the customised preparation with the poorest grade and the highest percentage of sugar content per 100 ml, determined according to paragraph 6 of the Sixteenth Schedule. [S 451/2023 wef 30/12/2023] |
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(4B) Where —(a) | a topping may be added to a freshly prepared Nutri-Grade beverage intended for sale in a specified setting; and | (b) | the topping is listed on a menu, poster, sign or other material that is used to inform a prospective consumer that the topping may be added to the Nutri-Grade beverage, |
then the person mentioned in paragraph (4) must (in addition to complying with that paragraph) ensure that a sugar declaration for each topping that may be added to the freshly prepared Nutri-Grade beverage — |
(c) | complies with the requirements for a nutrition information panel mentioned in paragraph (1); and | (d) | is available in any manner described in paragraph (5) to any person who wishes to view the information. [S 451/2023 wef 30/12/2023] |
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(4C) The requirement in paragraph (4B) may be satisfied in relation to a topping by a sugar declaration for the topping when the topping is added to any freshly prepared Nutri-Grade beverage sold in the specified setting, even if the person allows the topping to be added to more than one type of such beverage. [S 451/2023 wef 30/12/2023] |
(5) The information mentioned in paragraphs (4) and (4B) must be —(a) | if the Nutri-Grade beverage is sold from an automated beverage dispenser, clearly displayed on, or near to, the automated beverage dispenser; [S 451/2023 wef 30/12/2023] | (b) | on a website or other electronic record that is viewable by the person; or | (c) | on a physical document that is shown or given to the person on the person’s request. [S 451/2023 wef 30/12/2023] |
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(6) This regulation does not apply in respect of —(a) | any prepacked Nutri-Grade beverage that is not freshly prepared, has a total surface area of less than 100 square centimetres and bears a label that includes a statement of the quantity of total sugar and saturated fat; or [S 451/2023 wef 30/12/2023] | (b) | any of the following Nutri-Grade beverages, if the Nutri‑Grade beverage does not contain any calories, protein, fat, saturated fat, carbohydrate and sugar: (i) | coffee or a preparation of coffee; | (ii) | drinking water; | (iii) | a herbal infusion; | (iv) | tea or a preparation of tea. [S 993/2021 wef 30/12/2022] |
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184D.—(1) In these Regulations, “Nutri-Grade mark” means a mark indicating the following information for a Nutri-Grade beverage:(a) | its grade; | (b) | its percentage of sugar content per 100 ml, determined according to paragraph 6 of the Sixteenth Schedule and rounded to the nearest whole number. [S 451/2023 wef 30/12/2023] |
(2) [Deleted by S 451/2023 wef 30/12/2023] |
(3) A person required by regulation 184B(1) to ensure a prepacked Nutri-Grade beverage that is not freshly prepared and is intended for sale in a specified setting is graded —(a) | may label, or cause to be labelled, the package of a Nutri-Grade beverage with a Nutri-Grade mark if the Nutri-Grade beverage’s grade is “A” or “B”; | (b) | must ensure the package of a Nutri-Grade beverage is labelled with a Nutri-Grade mark if the Nutri-Grade beverage’s grade is “C” or “D”; and | (c) | if the package is labelled in accordance with sub‑paragraph (a) or (b), must ensure the Nutri-Grade mark is labelled on the front-of-pack (called in this regulation the FOP) of the package, that is, the face of the package —(i) | where the Nutri-Grade beverage’s name and brand (if there is a brand) appear; and | (ii) | that is in a prospective consumer’s principal field of vision. [S 451/2023 wef 30/12/2023] [S 451/2023 wef 30/12/2023] |
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(4) For the purpose of paragraph (3), where more than one unit of prepacked Nutri-Grade beverage is packaged for sale as a single item, the requirement to ensure the FOP of the package is labelled under that paragraph may be satisfied —(a) | by ensuring the FOP of the package to be sold as a single item is labelled with a Nutri-Grade mark in respect of each type of Nutri-Grade beverage within the package and the package includes a statement that each unit in the package must not be sold separately or a statement to the like effect; or | (b) | where the package to be sold as a single item is wholly transparent, by ensuring the FOP of each unit within the transparent package is labelled and ensuring that the Nutri-Grade mark is clearly visible through the transparent package. |
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(4A) Where a person is required by regulation 184B(1) to ensure a Nutri-Grade beverage intended for sale in a specified setting is graded and the person uses a menu, poster, sign or other material to inform a prospective consumer that the Nutri-Grade beverage is for sale —(a) | if the Nutri-Grade beverage’s grade is “A” or “B” — the person may label, or cause to be labelled, each listing of the Nutri-Grade beverage in the menu, poster, sign or other material with a Nutri-Grade mark that is either next to or in direct relation to each listing; or | (b) | if the Nutri-Grade beverage’s grade is “C” or “D” — the person must ensure that each listing of the Nutri-Grade beverage in the menu, poster, sign or other material is labelled with a Nutri-Grade mark that is either next to or in direct relation to each listing. [S 451/2023 wef 30/12/2023] |
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(4B) Where a person labels, or causes to be labelled, a menu, poster, sign or other material in accordance with paragraph (4A)(a), or is required to ensure a menu, poster, sign or other material is labelled in accordance with paragraph (4A)(b), the person must ensure —(a) | if the Nutri-Grade beverage is one for which a prospective consumer may customise the amount of at least one ingredient in the Nutri-Grade beverage — that the menu, poster, sign or other material includes a description of how the Nutri-Grade beverage that the Nutri-Grade mark is based on is customised; and | (b) | if a topping may be added to the freshly prepared Nutri-Grade beverage — that the menu, poster, sign or other material includes a sugar declaration in relation to the topping. [S 451/2023 wef 30/12/2023] |
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(4C) The requirement in paragraph (4B)(b) may be satisfied in respect of a topping by a sugar declaration for the topping when the topping is added to any freshly prepared Nutri-Grade beverage listed on the menu, poster, sign or other material, even if the person allows the topping to be added to more than one type of such beverage. [S 451/2023 wef 30/12/2023] |
(4D) Where a person sells a Nutri-Grade beverage in a specified setting from a consumer-facing automated beverage dispenser —(a) | if the Nutri-Grade beverage’s grade is “A” or “B” — the person may label, or cause to be labelled, the Nutri-Grade beverage with a Nutri-Grade mark in accordance with paragraph (4E); and | (b) | if the Nutri-Grade beverage’s grade is “C” or “D” — the person must ensure that the Nutri-Grade beverage is labelled with a Nutri-Grade mark in accordance with paragraph (4E). [S 451/2023 wef 30/12/2023] |
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(4E) For the purpose of paragraph (4D) —(a) | the label must be on, or near to, the automated beverage dispenser; and | (b) | if more than one beverage is available from the automated beverage dispenser, the label must be next to or in direct relation to the image or text listing of the Nutri-Grade beverage. [S 451/2023 wef 30/12/2023] |
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(5) A Nutri-Grade mark, and any sugar declaration under paragraph (4B)(b), must comply with the specifications in the document known as “Specifications of the Nutri Grade mark and Sugar Declaration” published by the Health Promotion Board, as in force from time to time. [S 993/2021 wef 30/12/2022] [S 451/2023 wef 30/12/2023] |
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184E. [Deleted by S 451/2023 wef 30/12/2023] |
Prohibition on advertisements relating to Nutri-Grade beverages graded “D” |
184F.—(1) A person must not publish, cause to be published, or take part in the publication of, any advertisement used or apparently used to promote, directly or indirectly, the sale of a Nutri-Grade beverage graded “D”. (2) Paragraph (1) does not apply to any advertisement —(a) | that does not contain a recommendation relating to the consumption of the Nutri-Grade beverage and is published by means of a catalogue, price list or other document for the purpose of supplying the Nutri-Grade beverage by wholesale; | (b) | that provides information about the Nutri-Grade beverage’s name or price or both but does not otherwise promote its sale and is published —(i) | on the corporate website of —(A) | a manufacturer, an importer or a distributor of a Nutri-Grade beverage that is not freshly prepared; or | (B) | a seller of a freshly prepared Nutri-Grade beverage; [S 451/2023 wef 30/12/2023] |
| (ii) | as part of a product launch that is not accessible to any member of the general public other than an invited guest; or | (iii) | in the form of a press or media release; [S 451/2023 wef 30/12/2023] [S 451/2023 wef 30/12/2023] |
| (c) | that complies with all of the following requirements:(i) | the advertisement is published at a variety shop or an online variety shop; | (ii) | the advertisement is for a prepacked Nutri-Grade beverage that is not freshly prepared; | (iii) | the advertisement displays an image of the Nutri-Grade beverage’s Nutri-Grade mark, except that an advertisement that involves communication in an audible message need not display the image but must include the audible message that “The Nutri-Grade of this product is D”; or [S 451/2023 wef 30/12/2023] |
| (d) | that is a menu, poster, sign or other material labelled in accordance with regulation 184D(4A) and (4B). [S 451/2023 wef 30/12/2023] |
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(3) In this regulation —“corporate website” means an Internet website of a manufacturer, an importer, a distributor or a seller (called in this definition A) that is accessible by the public and through which the public may obtain information about A or A’s products, but does not include a specified online location; |
“online variety shop” means an online location of sale that sells mainly the variety of things referred to in the definition of “variety shop”; |
“specified online location” means any part of an online location of sale where a prospective consumer is able to select for purchase a Nutri-Grade beverage intended for sale in a specified setting; |
“variety shop” includes a convenience store, grocery shop, supermarket or other establishment however named that sells mainly a variety of food, small household items, toiletries and other small consumer goods. [S 451/2023 wef 30/12/2023] |
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185.—(1) Intoxicating liquor shall be a liquor of any description containing more than 0.5% (v/v) alcohol at 20°C and which is fit, or intended or can by any means be converted for use as a beverage, and includes “toddy” but does not include denatured spirit.(2) No liquor for which medicinal properties are claimed shall be advertised, labelled or sold as food. |
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Ale, beer, lager, porter or stout |
186. Ale, beer, lager, porter or stout shall be a fermented liquid containing not less than 1.0% (v/v) alcohol at 20°C. It shall be brewed from a mash of malted or other grain and sugar or dextrose or both, with hops or other harmless vegetable bitters. |
187.—(1) Wine shall be the product solely of the alcoholic fermentation of the juice or must of grapes with or without the addition of pure grape spirit fortification.(2) Dry wine means wine produced by complete fermentation of the sugar contained in the juice or must of the grapes from which it is made. |
(3) Sweet wine means wine containing sugar derived only from the juice or must of the grapes from which it is made. |
(4) In these Regulations, the common name for wine shall also mean any words indicating the specific type of grapes from which the wine is made or the locality from which the grapes used originated or the locality in which the wine was made. |
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188. Malt wine, or any wine which purports to contain any malt extract, shall be wine conforming to the general standard for wine, to which has been added malt extract, so that the resultant wine contains not less than 5% (w/v) malt extract. |
189. Quinine wine shall be wine containing quinine or compounds of quinine (calculated as quinine hydrochloride) in proportion of not less than 0.5 and not more than 2.3 mg per ml. |
Aromatic wine, wine cocktail and vermouth |
190. Aromatic wine, wine cocktail and vermouth shall be wine to which has been added harmless botanical bitters, aromatics or other permitted flavouring agents. It may be coloured with caramel and may be sweetened with sugar, dextrose, invert sugar, raisins or other dried grapes. It shall contain not more than 24.0% (v/v) alcohol at 20°C. |
191. Port and sherry shall be fortified wines and shall contain not less than 17.0% (v/v) alcohol at 20°C. |
192. Meat wine or beef wine, or any wine which purports to contain any extract of meat or beef shall be wine conforming to the general standard for wine, to which has been added meat extract or beef extract, so that the resultant wine contains not less than 2% protein. |
193.—(1) Sparkling wine shall be wine that contains no carbon dioxide other than that generated intrinsically from ingredients during its manufacture.(2) The word “champagne” shall not be used in respect of produce which is carbonated in any way other than by the traditional method of fermentation in the bottle. |
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194. Carbonated wine shall be wine to which industrial carbon dioxide has been artificially added. |
195.—(1) Fruit wine shall be the product of the alcoholic fermentation of the juice, or of the juice and other portions of fruit other than grapes.(2) No fruit wine shall be labelled with the word “wine” unless the name of the fruit from which it is made immediately precedes the word “wine”. The name of the fruit shall be in letters of the same size and colour as the word “wine”. |
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196.—(1) Cider or perry shall be the product of the alcoholic fermentation of the juice or must of sound apples or pears, respectively.(2) The word “champagne” or any other words of similar meaning shall not be used in reference to cider and perry. |
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Sparkling cider or sparkling perry |
197. Sparkling cider or sparkling perry shall be cider or perry that contains no carbon dioxide other than that generated intrinsically from ingredients during its manufacture. |
Aerated cider or aerated perry |
198. Aerated cider or aerated perry means cider or perry that is impregnated either naturally or artificially with carbon dioxide under pressure. |
199. Honey wine shall be the product of the alcoholic fermentation of honey with or without the addition of caramel, harmless natural botanical flavours and honey spirit. |
Cereal grain wine and Chinese wine |
200.—(1) Cereal grain wine and Chinese wine or “chiew” (“jiu”) or “samsu” shall be the product of the alcoholic fermentation of any wholesome cereal grain.(2) No cereal grain “wine” or Chinese wine shall be labelled with the word “wine” unless the name of the cereal from which it is made or the Chinese name of the product is spelt out in English immediately preceding the word “wine”. The names shall be in letters of the same size and colour as those for the word “wine”. |
(3) Every container or receptacle containing cereal grain wine or Chinese wine shall bear a label indicating the alcohol content. |
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201.—(1) Brandy shall be the alcoholic distillate of the fermented juice of fresh grapes matured by storage in wood to develop its characteristics, without the admixture of any other spirits. [S 515/2006 wef 01/09/2006] (2) Brandy shall contain not less than 37.0% (v/v) alcohol at 20°C. |
(3) [Deleted by S 515/2006 wef 01/09/2006] |
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202. Marc brandy shall be the potable spirit distilled from the skin and pulp of grapes after the withdrawal of the juice of wine therefrom. |
203. Fruit brandy shall be the alcoholic distillate obtained by the distillation of —(a) | fruit wine or a mixture of fruit wines; | (b) | a mixture of wine and fruit wine; or | (c) | a fermented mash of sound ripe fruit or mixture of fruits or a mixture of such distillates. |
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204.—(1) Whisky shall be the alcoholic distillate obtained from a mash of cereal grain or cereal grain products matured by storage in wood to develop its characteristics, with or without the addition of caramel. [S 515/2006 wef 01/09/2006] (2) [Deleted by S 704/2020 wef 31/08/2020] |
(3) Flavoured whisky shall be whisky with the addition of permitted flavouring agent. |
(4) Whisky shall contain not less than 37.0% (v/v) alcohol at 20°C. |
(5) [Deleted by S 515/2006 wef 01/09/2006] |
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205.—(1) Rum shall be the alcoholic distillate obtained from sugar-cane products. It may contain caramel and may be flavoured with fruit or other harmless botanical substances or permitted flavouring agents.(2) Rum shall contain not less than 37.0% (v/v) alcohol at 20°C. |
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206.—(1) Gin, including Holland, Geneva and Genever shall be the product made from neutral spirit or suitably rectified spirit flavoured with the volatile products of juniper berries with or without other natural flavouring substances, and may contain sugar.(2) Dry Gin shall be gin to which no sugar has been added. |
(3) Gin of all varieties shall contain not less than 37.0% (v/v) alcohol at 20°C. |
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207.—(1) Vodka shall be the potable alcoholic beverage obtained from spirit and from carbohydrate and shall be without distinctive character, aroma or taste.(2) Vodka shall contain not less than 37.0% (v/v) alcohol at 20°C. |
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Liqueurs and alcoholic cordials |
208. Liqueurs and alcoholic cordials shall be obtained by the mixing or distillation of spirits with or over fruits, flowers, leaves or other harmless botanical substances or their juices, or with extracts derived by infusion, percolation or maceration of such botanical substances with or without permitted flavouring agent and colouring matter, and to which sucrose or dextrose or both have been added in an amount not less than 2.5% (w/v) of the finished product. |
209. Blended liquor shall be liquor consisting of a blend of a number of liquors each of which is separately entitled to the same generic description. |
210.—(1) Compounded liquor shall be liquor consisting of a number of different liquors not separately entitled to the same generic description. A compounded liquor shall not include in its nomenclature any geographic denomination of origin unless each of the different liquors comprising the compound is separately entitled to that geographic denomination.(2) No compounded liquor shall be labelled as liquor unless the name of the liquor is preceded by the word “compounded” which shall be in letters of the same size and colour as those for the name of the liquor. The label of such liquor shall, in addition to the normal requirement for liquor, include the words “Compounded in . . .” and in such blank space shall be specified the name of the country where the compounding was effected. |
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211. Salt, other than crude rock salt, shall be crystalline sodium chloride and shall contain on a dry basis not more than —(a) | 1.4% calcium sulphate; | (b) | 0.5% calcium and magnesium chlorides; and | (c) | 0.1% other matters insoluble in hot deci-normal solution of hydrochloric acid. |
Where the label contains a statement that the salt is free running, the salt may also contain not more than 2% of a permitted anti-caking agent. |
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212. Iodised salt shall be salt that contains potassium or sodium iodide or iodate in a proportion equivalent to not less than 25 and not more than 40 parts of iodide in every million parts of salt. |
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213. Spices (whether whole, partly ground or in powder form) and condiments are sound, aromatic vegetable substances used for flavouring of food, from which no portion of any oil or other flavouring substance, naturally contained in them, has been removed. [S 760/2022 wef 03/10/2022] |
214. [Deleted by S 760/2022 wef 03/10/2022] |
215. [Deleted by S 760/2022 wef 03/10/2022] |
216. [Deleted by S 760/2022 wef 03/10/2022] |
217. [Deleted by S 760/2022 wef 03/10/2022] |
218. [Deleted by S 760/2022 wef 03/10/2022] |
219. [Deleted by S 760/2022 wef 03/10/2022] |
220. [Deleted by S 760/2022 wef 03/10/2022] |
221. [Deleted by S 760/2022 wef 03/10/2022] |
222. [Deleted by S 760/2022 wef 03/10/2022] |
223. [Deleted by S 760/2022 wef 03/10/2022] |
224. [Deleted by S 760/2022 wef 03/10/2022] |
225. [Deleted by S 760/2022 wef 03/10/2022] |
226. [Deleted by S 760/2022 wef 03/10/2022] |
227. [Deleted by S 760/2022 wef 03/10/2022] |
228. [Deleted by S 760/2022 wef 03/10/2022] |
229. [Deleted by S 760/2022 wef 03/10/2022] |
230. [Deleted by S 760/2022 wef 03/10/2022] |
231. [Deleted by S 760/2022 wef 03/10/2022] |
232. [Deleted by S 760/2022 wef 03/10/2022] |
233. [Deleted by S 760/2022 wef 03/10/2022] |
234. [Deleted by S 760/2022 wef 03/10/2022] |
235. [Deleted by S 760/2022 wef 03/10/2022] |
236. [Deleted by S 760/2022 wef 03/10/2022] |
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FLAVOURING ESSENCES OR EXTRACTS |
237. [Deleted by S 760/2022 wef 03/10/2022] |
238. [Deleted by S 760/2022 wef 03/10/2022] |
239. [Deleted by S 760/2022 wef 03/10/2022] |
240. [Deleted by S 760/2022 wef 03/10/2022] |
241. [Deleted by S 760/2022 wef 03/10/2022] |
242. [Deleted by S 760/2022 wef 03/10/2022] |
243. [Deleted by S 760/2022 wef 03/10/2022] |
244. [Deleted by S 760/2022 wef 03/10/2022] |
245. [Deleted by S 760/2022 wef 03/10/2022] |
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246. [Deleted by S 760/2022 wef 03/10/2022] |
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247.—(1) In these Regulations, “special purpose food” shall be a food named or described as particularly suitable for consumption by persons belonging to a particular class who require a special diet. It shall be composed of food substance modified, prepared or compounded so as to possess nutritive and assimilative properties which render it specially suitable for use as food by these persons requiring the special diet.(2) Special purpose food shall include diabetic food, food containing added phytosterols, phytosterol esters, phytostanols or phytostanol esters, low sodium food, gluten-free food, low protein food, carbohydrate-modified food, low calorie food, energy food, infant formula food and formulated food. [S 195/2011 wef 15/04/2011] |
(3) Special purpose food may contain, unless otherwise prohibited under these Regulations, vitamins, minerals, amino acids and other nutrient supplements. |
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Labelling requirements for special purpose foods |
248.—(1) Every package of special purpose food, unless otherwise exempted, shall bear a label containing a nutrition information panel in the form specified in the Twelfth Schedule or in such other similar form as may be acceptable to the Director-General and adequate information to support any claim made for that food.(2) No package of a special purpose food that contains carbohydrate shall be labelled with the word “sugarless” or “sugar-free” or any words of similar meaning. |
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249. [Deleted by S 760/2022 wef 03/10/2022] |
250.—(1) Diabetic food shall be special purpose food that is particularly suitable for diabetics.(2) Every package of diabetic food shall be labelled with a nutrition information panel in the form specified in the Twelfth Schedule or in such other similar form as may be acceptable to the Director-General, and such nutrition information panel shall include a statement as to the nature of the carbohydrates present in the food. |
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Foods containing phytosterols, phytosterol esters, phytostanols or phytostanol esters |
250A.—(1) Food containing added phytosterols, phytosterol esters, phytostanols or phytostanol esters shall be special purpose food that is particularly suitable for persons who require a special diet for the purposes of lowering blood cholesterol levels.(2) Phytosterols, phytosterol esters, phytostanols or phytostanol esters may be added to —(a) | any edible vegetable fat or oil containing not more than 20 g of saturated fatty acids per 100 g of total fat; [S 152/2017 wef 01/04/2017] | (b) | any margarine or fat spread containing not more than 27 g of saturated fatty acids per 100 g of total fat; or [S 152/2017 wef 01/04/2017] | (c) | any other food containing not more than 3 g of total fat per 100 g or 1.5 g of total fat per 100 ml. [S 816/2014 wef 15/12/2014] |
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(3) Where any food with added phytosterols, phytosterol esters, phytostanols or phytostanol esters is sold or intended for sale, the can, bottle or other receptacle in which the food is contained shall have appearing thereon or attached thereto a label with the following statements or statements to the like effect:(a) | The product is a special purpose food intended for people who want to lower their blood cholesterol level; [S 816/2014 wef 15/12/2014] | (b) | [Deleted by S 816/2014 wef 15/12/2014] | (c) | The product may not be nutritionally appropriate for pregnant and breast-feeding women and children under the age of 5 years; | (d) | The product should be used as part of a balanced and varied diet; [S 816/2014 wef 15/12/2014] | (e) | Consumption in a day of a total of more than 3 g of phytosterols (whether in free form or as derived from any phytosterol esters) or phytostanols (whether in free form or as derived from any phytostanol esters), or both, does not provide any additional benefit in lowering blood cholesterol levels; [S 816/2014 wef 15/12/2014] | (f) | Consumption in a day of a total of at least 2 g of phytosterols (whether in free form or as derived from any phytosterol esters) or phytostanols (whether in free form or as derived from any phytostanol esters), or both, has been shown to lower blood cholesterol levels; and [S 816/2014 wef 15/12/2014] | (g) | A statement suggesting the amount of the food (in g or ml) to be consumed each time (referred to as a serving), and a statement of the total amount of phytosterols (whether in free form or as derived from any phytosterol esters) and phytostanols (whether in free form or as derived from any phytostanol esters) that each serving contains. [S 195/2011 wef 15/04/2011] [S 816/2014 wef 15/12/2014] |
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251.—(1) Infants’ food shall be any food described or sold as suitable for infants and shall include infant formula.(2) Infants’ food, other than infant formula formulated for infants from birth to 6 months of age, shall be food intended for feeding infants as a complementary food from over the age of 6 months, and shall be free from rancidity. [S 195/2011 wef 15/04/2011] |
(2A) No label or advertisement for infants’ food, other than infant formula formulated for infants from birth to 6 months of age, shall state or imply that such food is suitable for infants of or below 6 months of age. [S 195/2011 wef 15/04/2011] |
(3) Infants’ food shall not contain added mono-sodium salt of L-glutamic acid; and neither nitrates nor nitrites, other than those present naturally in foods, shall be used in any preparation of infants’ food. |
(4) Infants’ food shall not contain any chemical preservative. |
(5) Infants’ food shall be date-marked in accordance with regulation 10. |
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252.—(1) Infant formula shall be any food described or sold as an alternative to human milk for the feeding of infants. It shall be a product prepared from milk of cows or other animals or both or from other edible constituents of animals, including fish, or plants and which have been proved suitable for infant feeding.(2) Infant formula prepared in accordance with the directions on the label shall have an energy value of not less than 640 kcal and not more than 720 kcal per litre of the product ready for consumption. |
(3) Infant formula shall contain per 100 kcal of intake the following:(a) | not less than 1.8 g and not more than 4 g protein of nutritional quality equivalent to that of casein or greater quantity of other protein in proportion to its nutritional quality. The quality of the protein shall not be less than 85% of that of casein; | (b) | not less than 3.3 g and not more than 6 g fat and not less than 0.3 g linoleic acid in the form of glycerides; | (c) | not less than 75 mcg and not more than 150 mcg Vitamin A expressed as retinol; | (d) | not less than 40 and not more than 100 I.U. of Vitamin D; [S 195/2011 wef 15/04/2011] | (e) | not less than 8 mg Vitamin C (ascorbic acid); | (f) | not less than 40 mcg Vitamin B1 (thiamine); | (g) | not less than 60 mcg Vitamin B2 (riboflavin); | (h) | not less than 250 mcg nicotinamide; | (i) | not less than 35 mcg Vitamin B6. Formulae with a higher protein content than 1.8 g protein/100 kcal shall contain a minimum of 15 mcg Vitamin B6 per gram protein; | (j) | not less than 4 mcg folic acid; | (k) | not less than 300 mcg pantothenic acid; | (l) | not less than 0.15 mcg Vitamin B12; | (m) | not less than 4 mcg Vitamin K1; | (n) | not less than 1.5 mcg Vitamin H (Biotin); | (o) | not less than 0.7 I.U. Vitamin E (d-tocopherol compounds) per g linoleic acid (or per g polyunsaturated fatty acids, expressed as linoleic acid) but in no case less than 0.7 I.U./ 100 kcal; | (p) | not less than 20 mg and not more than 60 mg sodium (Na); | (q) | not less than 80 mg and not more than 200 mg potassium (K); | (r) | not less than 55 mg and not more than 150 mg chloride (Cl); | (s) | not less than 50 mg calcium (Ca) and the Calcium: Phosphorus (Ca:P.) ratio shall be not less than 1.2 and not more than 2.0; | (t) | not less than 25 mg of phosphorus (P) and the Calcium: Phosphorus (Ca:P.) ratio shall be not less than 1.2 and not more than 2.0; | (u) | not less than 6 mg magnesium (Mg); | (v) | not less than 0.15 mg iron (Fe); | (w) | not less than 5 mcg iodine (I); | (x) | not less than 60 mcg copper (Cu); | (y) | not less than 0.5 mg zinc (Zn); | (z) | not less than 5 mcg manganese (Mn); and | (za) | not less than 1 mcg and not more than 5 mcg selenium (Se). [S 195/2011 wef 15/04/2011] |
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(4) For the purpose of calculating the number of kilocalories supplied by a food referred to in this regulation —(a) | 1 g of any fat in that food shall be deemed to supply 9 kcal; | (b) | 1 g of any protein in that food shall be deemed to supply 4 kcal; | (c) | 1 g of any carbohydrate in that food shall be deemed to supply 4 kcal. |
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(5) Isolated amino acids may be added to infant formula only to improve its nutritional value. Essential amino acids may be added to improve protein quality, only in amounts necessary for that purpose. Only natural L-forms of amino acids shall be used. |
(6) The following ingredients may be added to infant formula in order to provide substances ordinarily found in human milk and to ensure that the formulation is suitable as the sole source of nutrition for the infant or to provide other benefits that are similar to outcomes of populations of breastfed babies:(a) | Nucleotides listed below, provided that the total level of nucleotides (including added and endogenous nucleotides) shall not exceed 16 mg per 100 kcal:(i) | Cytidine 5’-Monophosphate; | (ii) | Uridine 5’-Monophosphate; | (iii) | Adenosine 5’-Monophosphate; | (iv) | Guanosine 5’-Monophosphate; and | (v) | Inosine 5’-Monophosphate; |
| (b) | Long chain (20 and 22 carbon atoms) polyunsaturated fatty acids (LCP) but their content shall not exceed —(i) | 1% of the total fat content for n-3 LCP; and | (ii) | 2% of the total fat content for n-6 LCP (1% of the total fat content for arachidonic acid), |
and the eicosapentaenoic acid (20:5 n-3) content shall not exceed that of docosahexaenoic (22:6 n-3) acid content; |
| (c) | Galacto-oligosaccharides, long chain inulin and oligofructose produced from inulin, in an amount not exceeding a total level of 0.8 g per 100 ml; | (d) | Polydextrose, in an amount not exceeding a total level of 0.2 g per 100 ml; [S 493/2013 wef 01/08/2013] | (e) | Bovine lactoferrin, in an amount not exceeding 100mg per 100ml; [S 49/2016 wef 02/02/2016] [S 195/2011 wef 15/04/2011] [S 152/2017 wef 01/04/2017] | (f) | Beta-palmitin, with at least 52% of total palmitic acid esterified at the beta position, in an amount not exceeding 80% of the total fat content of infant formula; [S 152/2017 wef 01/04/2017] [S 146/2018 wef 28/03/2018] | (g) | 2’‑fucosyllactose, in an amount not exceeding 120 mg per 100 ml; [S 146/2018 wef 28/03/2018] | (h) | Lacto‑N‑neotetraose, in an amount not exceeding 60 mg per 100 ml; [S 146/2018 wef 28/03/2018] [S 695/2021 wef 01/10/2021] | (i) | 2’‑fucosyllactose/difucosyllactose mixture that contains at least 75% (w/w) 2’‑fucosyllactose and 5% (w/w) difucosyllactose, and that is —(i) | in the case of infant formula for an infant of or below 6 months of age — in an amount not exceeding 160 mg per 100 ml; or | (ii) | in the case of infant formula for an infant above the age of 6 months but not more than 12 months of age — in an amount not exceeding 120 mg per 100 ml; [S 695/2021 wef 01/10/2021] |
| (j) | Lacto‑N‑tetraose that is —(i) | in the case of infant formula for an infant of or below 6 months of age — in an amount not exceeding 80 mg per 100 ml; or | (ii) | in the case of infant formula for an infant above the age of 6 months but not more than 12 months of age — in an amount not exceeding 60 mg per 100 ml. [S 695/2021 wef 01/10/2021] |
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(7) In the case of infant formula that is sold or to be sold as infant formula which is lactose free, low lactose or words of similar import, the total lactose content must not be greater than 10 mg per 100 kcal. [S 580/2019 wef 01/09/2019] |
(8) [Deleted by S 195/2011 wef 15/04/2011] |
(9) [Deleted by S 195/2011 wef 15/04/2011] |
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Infant milk formula or infant milk preparation |
253. Infant milk formula or infant milk preparation shall be infant formulae prepared from cow’s milk. It may have part or whole of its butterfat replaced by vegetable oils. It shall comply with the standards laid down for infant formula. |
Labelling of infant formula |
254.—(1) Every package of infant formula, other than infant milk formula, shall bear a label indicating the sources of protein. Such indication shall be printed immediately after the common name “infant formula” or any appropriate designation.(2) There shall be printed on the label for infant formula —(a) | directions as to the method of preparing the food; | (aa) | a warning statement about the health hazards of improper use, preparation or storage of infant formula; [S 580/2019 wef 01/09/2019] | (b) | the amount of energy and the number of grams of protein, fat and carbohydrate per 100 ml or other equivalents of formula prepared in accordance with the directions on the label; | (c) | the total quantity of each vitamin and mineral per 100 ml or other equivalents of formula prepared in accordance with the directions on the label; | (d) | a statement suggesting the amount of the prepared food to be given each time, and the number of times such amount is to be given per day; such statement shall be given for each month of the infants’ age up to 6 months; | (e) | directions for storage and information regarding its keeping qualities before and after the container has been opened; [S 580/2019 wef 01/09/2019] | (f) | information that infants above the age of 6 months should start to receive supplemental foods in addition to the formula, where the infant formula is intended for infants above the age of 6 months; and [S 302/2017 wef 15/06/2017] [S 580/2019 wef 01/09/2019] | (g) | prominently displayed statements, starting with the words “IMPORTANT NOTICE” or words of similar import, to ensure that a consumer understands that —(i) | breast milk is best for infants; and | (ii) | the infant formula should be used on the advice of a doctor or healthcare practitioner. [S 580/2019 wef 01/09/2019] |
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(3) Without limiting paragraph (2), the label on a package of any infant formula for infants, or an advertisement about any infant formula for infants, must not (and without affecting regulations 8A, 9, 9A, 9B, 11 and 12) contain —(a) | a claim which states, suggests or implies that the infant formula or a component, ingredient, constituent or other feature of the infant formula, has, or may have, a health effect; | (b) | a claim which directly or indirectly compares the infant formula, or a component, ingredient, constituent or other feature of the infant formula, to breast milk; | (c) | any of the following prohibited matter:(i) | a pictorial, graphic or symbolic representation of an infant or infants (whether or not accompanied by text); | (ii) | a pictorial, graphic or symbolic representation of a pregnant woman or nursing woman (whether or not accompanied by text); | (iii) | a word like “humanised” or “maternalised”, or words of similar import; | (iv) | a claim which directly or indirectly idealises the use or effect of the infant formula;Example of idealisation claims |
| A representation which suggests or implies that the use or consumption of the infant milk formula results in exaggerated health or other effect. |
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| (d) | a claim which states, suggests or implies the energy, carbohydrate and other nutritive property of any ingredient of the infant formula which is not mentioned in regulation 252(5) and (6), except to the extent permitted by paragraph (4) or (5);Examples of prohibited text claims |
| | (b) | “Contains essential nutrients”. |
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| (c) | “Added with vitamins and minerals”. |
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| (e) | where the infant formula contains any ingredient mentioned in regulation 252(5) or (6), a claim which states, suggests or implies that the infant formula is enriched or fortified, or is an excellent source of these ingredients;Examples of prohibited text claims |
| (a) | “Excellent source of DHA”. |
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| | (c) | “High in nucleotides”. |
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| (d) | “Enriched with nucleotides”. |
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[S 580/2019 wef 01/09/2019] |
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(4) A label on any package of any infant formula, or an advertisement about any infant formula, may contain a claim which states, suggests or implies the presence of hydrolysed milk protein or whey protein in the infant formula. [S 580/2019 wef 01/09/2019] |
(5) Without limiting paragraph (2), the label on a package of any infant formula which is sold or to be sold as lactose free or low lactose must (and without affecting regulations 8A, 9, 9A, 9B, 11 and 12) include —(a) | the words “lactose free” or “low lactose”, or words of similar import; | (b) | a statement within the nutrition information panel on the label, specifying the exact amount of lactose in the infant formula; and | (c) | the words “Not suitable for infants with galactosaemia” in the same font and size as, and in close proximity to, the words mentioned in sub‑paragraph (a), if the infant formula is manufactured from protein sources other than soya protein isolates. [S 580/2019 wef 01/09/2019] |
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(6) In paragraphs (3) and (4) —“claim” means any message or representation, and includes a pictorial, graphic or symbolic representation; |
“health effect” means an effect on the human body, including an effect on one or more of the following:(a) | growth and development; | (b) | physical performance; | (c) | mental performance; | (d) | a biochemical process or outcome; | (e) | a physiological process or outcome; | (f) | a functional process or outcome; |
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“pictorial representation” includes a graphic representation and an anthropomorphic or humanlike depiction. [S 580/2019 wef 01/09/2019] |
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