The Code of Federal Regulations of the United States of AmericaU.S. Government Printing Office, 1966 The Code of Federal Regulations is the codification of the general and permanent rules published in the Federal Register by the executive departments and agencies of the Federal Government. |
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Pagina 19
... manufacturing history of the package of the drug ; Provided , however , That in the case of containers too small or otherwise unable to accommodate a label with sufficient space to bear all such information , but which are packaged ...
... manufacturing history of the package of the drug ; Provided , however , That in the case of containers too small or otherwise unable to accommodate a label with sufficient space to bear all such information , but which are packaged ...
Pagina 20
... manufacture , transportation , storage , or wholesale or retail distribution of veterinary drugs and is to be sold ... manufacturing history of the package of the drug ; Provided , however , That in the case of containers too small or ...
... manufacture , transportation , storage , or wholesale or retail distribution of veterinary drugs and is to be sold ... manufacturing history of the package of the drug ; Provided , however , That in the case of containers too small or ...
Pagina 23
... manufacture . A drug in a bulk package ( except tablets , capsules , or other dosage unit forms ) or a device ... manufacturing , processing , or repacking ” is immediately supplemented by the words " in the prep- aration of a new ...
... manufacture . A drug in a bulk package ( except tablets , capsules , or other dosage unit forms ) or a device ... manufacturing , processing , or repacking ” is immediately supplemented by the words " in the prep- aration of a new ...
Pagina 37
... manufacturing processes or controls . The Director of the Bureau of Medicine , the Director of the Division of New Drugs , and the Di- rector of the Bureau of Veterinary Medi- cine are authorized to notify applicants of supplements to ...
... manufacturing processes or controls . The Director of the Bureau of Medicine , the Director of the Division of New Drugs , and the Di- rector of the Bureau of Veterinary Medi- cine are authorized to notify applicants of supplements to ...
Pagina 38
... manufacturers , packers , and distributors of glandular prepara- tions . Notice to manufacturers , packers , and distributors of drugs for internal use which contain mineral oil . Disposition of incubator reject eggs . Notice to ...
... manufacturers , packers , and distributors of glandular prepara- tions . Notice to manufacturers , packers , and distributors of drugs for internal use which contain mineral oil . Disposition of incubator reject eggs . Notice to ...
Alte ediții - Afișează-le pe toate
The Code of Federal Regulations of the United States of America ..., Volumul 1 Vizualizare completă - 1939 |
The Code of Federal Regulations of the United States of America ..., Volumul 3 Vizualizare completă - 1939 |
Termeni și expresii frecvente
0.5 percent 52 Stat added amended artificial coloring artificial flavoring batch bear the statement benzoyl peroxide blank being filled calcium calcium chloride certification colby cheese color additive conspicuously precede corn sirup Cosmetic Act cream curd D&C Red definition and standard dextrose dosage dried dye as determined exempt Federal Food flour Food and Drug glucose glucose sirup graphic matter gredients ingredients specified intervening written invert sugar sirup label shall bear label so conspicuously label statement matter at 135 method prescribed milk fat milligrams mixture moisture muenster cheese optional ingredients orange juice oysters package packing medium pasteurized process cheese percent by weight precede or follow prepared process cheese Pure dye quantity rennet salt seen under customary sieve sirup sodium sorbate solids sorbic acid specified in paragraph spice standard of identity statement of optional subparagraph tion titanium trichloride tity units vegetable wheat Wherever the name word
Pasaje populare
Pagina 663 - Statistical Reporting Service, Agriculture Department Subversive Activities Control Board Tariff Commission, United States Tax Court of the United States Tennessee Valley Authority Trade Negotiations, Office of Special Representative Transport Mobilization Staff, Interstate Commerce Commission Transportation, Office of Under Secretary of Commerce for Transportation and Communications Service Treasury Department Coast Guard Comptroller of the Currency, Bureau of Customs Bureau Federal Procurement...
Pagina 6 - Presentation of views under section 305 of the act shall be private and informal. The views presented shall be confined to matters relevant to the contemplated proceeding. Such views may be presented by letter or in person by the person to whom the notice was given, or by his representative. In case such person holds a guaranty or undertaking referred to in section 303 (c) (2) or (3) of the act applicable to the article on which such notice was based, such guaranty or undertaking, or a verified copy...
Pagina 21 - ... recommendations for use of the drug. (5) All labeling, except labels and cartons, bearing information for use of the drug also bears the date of the issuance or the date of the latest revision of such labeling. (6) A prescription drug intended for both human and veterinary use shall comply with paragraph (b) of this section and subparagraphs (4) and (5) of this paragraph. (d) Exemption for prescription devices. A device which, because of any potentiality for harmful effect, or the method of its...
Pagina 11 - In such labeling by a name which includes or suggests the name of one or more but not all such Ingredients, even though the names of all such Ingredients are stated elsewhere In the labeling.
Pagina 24 - ... will not be adulterated or misbranded within the meaning of the Act upon completion of such processing, labeling, or repacking. Such person and such operator, shall each keep a copy of such agreement until 2 years after the final shipment or delivery of such...
Pagina 28 - Except as provided by paragraphs (e) and (f) of this section, a shipment or other delivery of a food which is, in accordance with the practice of the trade, to be processed, labeled, or repacked in substantial quantity at an establishment other than that where originally processed or packed, shall be exempt, during the time of introduction into and movement in interstate commerce and the time of holding in such establishment, from compliance with the labeling requirements of...
Pagina 52 - Section 403 (g) (2) (requiring the label of a food which purports to be or is represented as one for which a definition and standard of identity has been prescribed to bear the name of the food specified in the definition and standard and, insofar as may be required by the regulation establishing the standard the common names of the optional ingredients present in the food) , if the food...
Pagina 27 - ... of the act by reason (among other reasons) of: (1) The failure of such word, statement, or information to appear on the part or panel of the label which is presented or displayed under customary conditions of purchase; (2) The failure of such word, statement, or information to appear on two or more parts or panels of the label, each of which has sufficient space therefor, and each of which is so designed as to render it likely to be, under customary conditions of purchase, the part or panel displayed;...
Pagina 271 - When optional ingredient (a) (1) is used, the label shall bear the word "spiced" or the statement "spice added" or "with added spice"; but in lieu of the word "spice" in such statements the common name of the spice may be used. (2) When optional ingredient (a) (5) is used, the label shall bear the words "sodium benzoate" or "benzoic acid," or "sodium benzoate and benzoic acid," as the case may be, followed by the words "added as preservative.
Pagina 310 - Tomatoes" and any statements required or authorized to appear with such name by § 53.40 (b). § 53.42 Canned tomatoes, fill of container; label statement of substandard fill, (a) The standard of fill of container for canned tomatoes is a fill of not less than 90 percent of the total capacity of the container, as determined by the general method for fill of containers prescribed in § 10.2 (b) of this chapter.