Versão HTML básica
40
ANEXO 1 – REFERÊNCIAS REGULATÓRIAS
• Federal Food, Drug and Cosmetic Act (FD&C Act).
• Fair Packaging and Labeling Act (FP&L Act).
• Toxic Substances Control Act (TSC Act).
• Bacteriological Analytical Manual, Chapter 23, Microbiological Methods for
Cosmetics.
• Code of Federal Regulation (CFR):
• Title 21 CFR part 1.21 – Failure to reveal material facts.
• Title 21 CFR part 1.24 – Exemptions from required label statements.
• Title 21 CFR part 73 – Listing of color additives exempt from certification.
• Title 21 CFR part 74 – Listing of color additives subject to certification.
• Title 21 CFR part 80 – Color additive certification.
• Title 21 CFR part 81 – General specifications and restrictions for provisional
color additives.
• Title 21 CFR part 82 – Listing of certified provisionally listed colors and speci-
fications.
• Title 21 CFR part 207 – Registration of producers of drugs and listing of drugs
in commercial distribution.
• Title 21 CFR part 210 and 211 – Current good manufacturing practice for drugs.
• Title 21 CFR part 250.250 Hexachlorophene, as a component of drug and cos-
metic products.
• Title 21 CFR part 300 to 314 – New drugs approval.
• Title 21 CFR part 347 – Skin protectant drug products for OTC human use.
• Title 21 CFR part 350 – Antiperspirant drug products for OTC human use.
• Title 21 CFR part 352 – Sunscreen drug products for OTC human use.
• Title 21 CFR part 355 – Anticaries drug products for OTC human use.
• Title 21 CFR part 710 – Voluntary registration of cosmetic product establish-
ments.
• Title 21 CFR part 720 – Voluntary filing of cosmetic product ingredient com-
position statements.
• Title 21 CFR part 701.20 – Detergent substances, other than soap, intended for
use in cleansing the body.
• Title 21 CFR part 701.13 – Declaration of net quantity of contents.