An ingredient definition

An ingredient means any chemical substance of synthetic or natural origin which is deliberately added to the cleaning product. For the purposes of this Annex, a per- fume, essential oil or colouring agent is deemed to be an individual ingredient unless it contains an allergenic fragrance as specified in Number 3 paragraph 4. 2 Prohibitions1 It is prohibited to produce for personal use or place on the market cleaning prod- ucts containing: 131 Revised by No I 3 of the O of 15 Dec. 2006 (AS 2007 111), No I of the O of 13 Feb. 2008 (AS 2008 561), Annex No 2 of the O of 14 Jan. 2009 (AS 2009 401), No I of the FOEN Ordinance of 19 Oct. 2009 (AS 2009 5429), No I 6 of the O of 10 Dec. 2010 (AS 2011 113), No II para. 3 of the O of 7 Nov. 2012 (AS 2012 6161) and No II para. 2 of the O of 1 July 2015, in force since 1 Sept. 2016 (AS 2015 2367). The correction of 20 June 2017 relates to the French and Italian texts only (AS 2017 3541).
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An ingredient means any chemical substance of synthetic or natural origin which is deliberately added to the detergent. For the purposes of this Annex, a perfume, essential oil or colouring agent is deemed to be an individual ingredient unless it contains an allergenic fragrance as specified in Number 3 paragraph 4. 2 Prohibitions1 It is prohibited to produce for personal use or place on the market laundry deter- gents containing:
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An ingredient means any chemical substance of synthetic or natural origin which is deliberately added to the cleaning product. For the purposes of this Annex, a per- fume, essential oil or colouring agent is deemed to be an individual ingredient unless it contains an allergenic fragrance as specified in Number 3 paragraph 4.
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Examples of An ingredient in a sentence

  • An ingredient, impurity, or contaminant present in a covered product as an unintentional consequence of manufacturing and which has no functional or technical effect on the finished product.

  • An ingredient not in common use in food prior to January 1, 1958, may achieve general recognition of safety only through scientific procedures.

  • An ingredient which is both fragrance and flavor shall be designated by each of the functions it performs unless such ingredient is identified by name.

  • An ingredient, impurity, or contaminant present in a covered product as an unintentional consequence of manufacturing and which has no functional or technical effect on the finished productThe following Designated Lists are only referenced in the state of New York’s HCPIDP Regulation*: 24, 25, 26, 27, 28, 29.

  • An ingredient, impurity, or contaminant present in a covered product as an unintentional consequence of manufacturing and which has no functional or technical effect on the finished product (Appendix D).

  • An ingredient or other constituent of a food that will not be further treated or otherwise processed to control the most resistant microorganism of public health significance.

  • An ingredient, in a hermetically sealed and unopened container, that is commercially processed to achieve and maintain commercial sterility under conditions of nonrefrigerated storage and distribution.

  • An ingredient combined with marihuana to prepare topical or oral administrations, food, drink, or other products.

  • An ingredient statement is not required for single standardized ingredient feeds which are officially defined.(d) The name and principal mailing address of the man- ufacturer or the person responsible for distributing the com- mercial feed.(e) Adequate directions for use for all commercial feeds containing drugs and for all such other commercial feeds as the department may require by rule as necessary for their safe and effective use.

  • An ingredient developed in the US is not necessarily tested in the US.

Related to An ingredient

  • Inert ingredient means an ingredient which is not an active ingredient.

  • Active Ingredient means any com- ponent that is intended to furnish pharmacological activity or other di- rect effect in the diagnosis, cure, miti- gation, treatment, or prevention of dis- ease, or to affect the structure or any function of the body of humans. The term includes those components that may undergo chemical change in the manufacture of the drug product and be present in the drug product in a modified form intended to furnish the specified activity or effect.

  • ingredient means any substance, including a food additive used in the manufacture or preparation of food and present in the final product, possibly in a modified form;

  • Active Pharmaceutical Ingredient or “API” shall mean one or more of the following active pharmaceutical ingredients: tenofovir alafenamide (“TAF”), tenofovir disoproxil fumarate (“TDF”), elvitegravir (“EVG”), and cobicistat (“COBI”).

  • Biological Samples means any physical samples obtained from Study Participants in accordance with the Protocol for the purposes of the Study.

  • Additives means non-hydrocarbon compounds added to or blended with a product to modify its properties;

  • Bulk drug substance means any substance that is represented for use, and that, when used in the

  • Food and food ingredients means substances, whether in liquid, concentrated, solid, frozen, dried, or dehydrated form, that are sold for ingestion or chewing by humans and are consumed for their taste or nutritional value. Food and food ingredients do not include alcoholic beverages and tobacco.

  • Bulk Product means Licensed Product supplied in a form other than Finished Product which can be converted into Finished Product.

  • Radioactive Products or Waste means any radioactive material produced in, or any material made radioactive by exposure to the radiation incidental to the production or utilization of nuclear fuel, but does not include radioisotopes which have reached the final stage of fabrication so as to be usable for any scientific, medical, agricultural, commercial or industrial purpose.

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Pharmaceutical Product shall have the meaning ascribed to such term in Section 3.1(hh).

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • Finished Products means any one or more of the following petroleum oils, or a mixture or combination of these oils, to be used without further processing except blending by mechanical means:

  • API means American Petroleum Institute.

  • Packaged means bottled, canned, cartoned, or securely wrapped.

  • Products means information resources technologies that are, or are related to, EIR.

  • Aerosol coating product means a pressurized coating product containing pigments or resins that dispenses product ingredients by means of a propellant, and is packaged in a disposable can for hand-held application, or for use in specialized equipment for ground traffic/marking applications.

  • Fluoroscopic imaging assembly means a subsystem in which X-ray photons produce a visual image. It includes the image receptor(s) such as the image intensifier and spot-film device, electrical interlocks, if any, and structural material providing linkage between the image receptor and diagnostic source assembly.

  • Product Specifications means the specifications, features and/or terms of any "Contract" (as defined in the LME Rules) listed for trading on the LME, as described in the LME Rules;

  • MSAA Indicator Technical Specifications document means, as the context requires, either or both of the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Indicator Technical Specifications November 5, 2018 Version 1.3” and the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Target and Corridor-Setting Guidelines” as they may be amended or replaced from time to time;

  • Radioactive material means any solid, liquid, or gas which emits radiation spontaneously.

  • Explosive material means any chemical compound, mixture, or device which produces a substantial instantaneous release of gas and heat spontaneously or by contact with sparks or flame.

  • Raw Materials means all raw materials, supplies, components and packaging necessary to manufacture and ship the Product in accordance with the Specifications, as provided in Exhibit A, but not including the API.

  • Biological product means a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, allergenic product, protein other than a chemically synthesized polypeptide, or analogous product, or arsphenamine or any derivative of arsphenamine or any other trivalent organic arsenic compound, applicable to the prevention, treatment, or cure of a disease or condition of human beings.