Label: HYDROQUINONE 5% / TRETINOIN 0.025% / TRIAMCINOLONE ACETONIDE 0.025% emulsion
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-6117-2 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated May 20, 2019
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- Sincerus Florida, LLC. Adverse reactions
- Active, inactive
- NDC 72934- 6117-2 HYDROQUINONE USP 5% / TRETINOIN USP 0.025% / TRIAMCINOLONE ACETONIDE USP 0.025%. Emulsion 30 gm
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INGREDIENTS AND APPEARANCE
HYDROQUINONE 5% / TRETINOIN 0.025% / TRIAMCINOLONE ACETONIDE 0.025%
hydroquinone 5% / tretinoin 0.025% / triamcinolone acetonide 0.025% emulsionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-6117 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE 5 g in 100 g TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN 0.025 g in 100 g TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (TRIAMCINOLONE ACETONIDE - UNII:F446C597KA) TRIAMCINOLONE ACETONIDE 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:72934-6117-2 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/20/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/20/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-6117)
