Label: 141016 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025% emulsion
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-6225-2 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated July 2, 2020
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- Sincerus Florida, LLC adverse reactions
- Active, inactive
- NDC 72934-6225-2 141016 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025% emulsion 30 gm
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INGREDIENTS AND APPEARANCE
141016 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025%
141016 hydrocortisone 0.5% / hydroquinone 4% / tretinoin 0.025% emulsionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-6225 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE 4 g in 100 g HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 0.5 g in 100 g TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN 0.025 g in 100 g Product Characteristics Color yellow Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-6225-2 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/02/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/02/2020 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-6225)
