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: 107 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 only to the French and Italian texts (AS 2017 3541).
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:

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 product (Appendix D).

  • 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 or a container of refrigerated, ready-to-eat, potentially hazardous food specified in paragraph 64E- 11.004(14)(b), F.A.C., shall be discarded if not sold or served within 7 calendar days, excluding the time that the product is frozen, after the original package is opened or by the manufacturer’s “sell by” or “use by” date, whichever occurs first, if the manufacturer determined the date based on food safety.

  • 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 cannot be the same time nutrient and additive.For example, L-ascorbic acid used as a chemical form of a nutrient (Vitamin C) or ascorbic acid used as additive E300.You must choose in Foodsup nutrients under the type “chemical form of nutrient” in the search engine and the type “additive” for additives.

  • 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 mentioned in a common name of a food should be present in a significant proportion.

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”).

  • Bulk drug substance means any substance that is represented for use, and that, when used in the compounding, manufacturing, processing, or packaging of a drug, becomes an active ingredient or a finished dosage form of the drug; however, "bulk drug substance" shall not include intermediates that are used in the synthesis of such substances.

  • 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 set of fluoroscopic images or radiographic images recorded from the fluoroscopic image receptor. It includes the image receptors, electrical interlocks, if any, and structural material providing linkage between the image receptor and diagnostic source assembly.

  • Product Specifications means the quality and other specifications set forth on Appendix 2 to this Agreement.

  • 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 goods, excluding equipment and machinery, purchased for use in manufacturing a product.

  • 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.

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Therapeutically equivalent drug products means drug products that contain the same active