Code of Federal Regulations Title 21. Food and Drugs § 21.74.1336 D&C Red No. 36

(a) Identity.

(b) Specifications. D&C Red No. 36 shall conform to the following specifications and shall be free from impurities other than those named to the extent that such impurities may be avoided by current good manufacturing practice:

Volatile matter at 135 °C (275 °F), not more than 1.5 percent.

Matter insoluble in toluene, not more than 1.5 percent.

2–Chloro–4–nitrobenzenamine, not more than 0.3 percent.

2–Naphthalenol, not more than 1 percent.

2,4–Dinitrobenzenamine, not more than 0.02 percent.

1–[ (2,4–Dinitrophenyl)azo]–2–naphthalenol, not more than 0.5 percent.

4–[ (2–Chloro–4–nitrophenyl)azo]–1–naphthalenol, not more than 0.5 percent.

1–[ (4–Nitrophenyl)azo]–2–naphthalenol, not more than 0.3 percent.

1–[ (4–Chloro–2–nitrophenyl)azo]–2–naphthalenol, not more than 0.3 percent.

Lead (as Pb), not more than 20 parts per million.

Arsenic (as As), not more than 3 parts per million.

Mercury (as Hg), not more than 1 part per million.

Total color, not less than 95 percent.

(c) Uses and restrictions. The color additive D&C Red No. 36 may be safely used for coloring ingested drugs, other than mouthwashes and dentifrices, in amounts not to exceed 1.7 milligrams per daily dose of the drug for drugs that are taken continuously only for less than 1 year. For drugs taken continuously for longer than 1 year, the color additive shall not be used in amounts to exceed 1.0 milligram per daily dose of the drug. D&C Red No. 36 may be safely used for coloring externally applied drugs in amounts consistent with current good manufacturing practice.

(d) Labeling requirements. The label of the color additive and any mixtures prepared therefrom intended solely or in part for coloring purposes shall conform to the requirements of § 70.25 of this chapter.

(e) Certification. All batches of D&C Red No. 36 shall be certified in accordance with regulations in part 80 of this chapter.