Code of Federal Regulations: Containing a Codification of Documents of General Applicability and Future Effect as of December 31, 1948, with Ancillaries and IndexDivision of the Federal Register, the National Archives, 1965 Special edition of the Federal Register, containing a codification of documents of general applicability and future effect ... with ancillaries. |
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Página 19
... components . ( b ) Color additives may be designated as coloring without naming specific color ice components unless the naming of such er components is required by a color addi- tive regulation prescribed in Part 8 of this chapter ...
... components . ( b ) Color additives may be designated as coloring without naming specific color ice components unless the naming of such er components is required by a color addi- tive regulation prescribed in Part 8 of this chapter ...
Página 20
... components unless the naming of such components is required by a color additive regulation prescribed in Part 8 of this chapter . ( c ) Trace amounts of harmless sub- stances added solely for individual prod- uct identification need not ...
... components unless the naming of such components is required by a color additive regulation prescribed in Part 8 of this chapter . ( c ) Trace amounts of harmless sub- stances added solely for individual prod- uct identification need not ...
Página 22
... components . A drug prepared , packaged , and primarily sold as a prescription chemical or other component for use by registered pharma- cists in compounding prescriptions or for dispensing in dosage unit form upon prescriptions shall ...
... components . A drug prepared , packaged , and primarily sold as a prescription chemical or other component for use by registered pharma- cists in compounding prescriptions or for dispensing in dosage unit form upon prescriptions shall ...
Página 43
... component in human drugs under the exemption pro- vided in § 1.106 ( k ) of this chapter or labeled for manufacturing use under the exemption provided in § 1.106 ( 1 ) will be regarded as misbranded unless the label bears the statement ...
... component in human drugs under the exemption pro- vided in § 1.106 ( k ) of this chapter or labeled for manufacturing use under the exemption provided in § 1.106 ( 1 ) will be regarded as misbranded unless the label bears the statement ...
Página 56
... component of dietary supplements , provided the di- rections for use are such that , when followed , daily ingestion will not exceed 0.1 milligram of the additive . ( b ) Preparations supplying over 0.1 milligram of pteroylglutamic acid ...
... component of dietary supplements , provided the di- rections for use are such that , when followed , daily ingestion will not exceed 0.1 milligram of the additive . ( b ) Preparations supplying over 0.1 milligram of pteroylglutamic acid ...
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Términos y frases comunes
0.2 percent 52 Stat acetate acid added alcohol amended Amprolium artificial bacitracin bear the statement blank being filled calcium certification cheese chickens chloride Chlortetracycline colby cheese color additive combination copolymer corn sirup Cosmetic Act curd D&C Red definition and standard dried ethylene exceed exemption extract Federal Food flavoring flour food additive Food and Drug fruit glucose sirup glycol grams gredients Hygromycin ingredients specified label shall bear label statement manufacturing ment method prescribed methyl milligrams milliliters million mixture Nystatin optional ingredients oxide Oxytetracycline oysters package packing pasteurized percent by weight Polyoxyethylene Polysorbate 60 potassium prepared principal ingredient process cheese quantity regulations resins safely salt sample shrimp sieve sirup skim milk sodium solids sorbitan specified in paragraph spice standard of identity statement of optional subparagraph Subpart substances sugar sulfate tion titanium trichloride tolerances for residues tylosin units