Label: 011312 NIACINAMIDE 4% / TAZAROTENE 0.05% cream
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-2208-2 - 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 72934-2208-2 011312 NIACINAMIDE 4% / TAZAROTENE 0.05% cream 30 gm
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INGREDIENTS AND APPEARANCE
011312 NIACINAMIDE 4% / TAZAROTENE 0.05%
011312 niacinamide 4% / tazarotene 0.05% creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-2208 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TAZAROTENE (UNII: 81BDR9Y8PS) (TAZAROTENE - UNII:81BDR9Y8PS) TAZAROTENE 0.05 g in 100 g NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 4 g in 100 g Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-2208-2 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(72934-2208)
