Label: FLUTICASONE PROPIONATE 0.05% / NIACINAMIDE 4% cream
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Updated May 13, 2019
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- Directions for use
- Sincerus Florida, LLC. Adverse reactions
- Active, inactives
- NDC 72934- 2087-2 FLUTICASONE PROPIONATE USP 0.05% / NIACINAMIDE USP 4%. Cream 30gm.
INGREDIENTS AND APPEARANCE
FLUTICASONE PROPIONATE 0.05% / NIACINAMIDE 4%
fluticasone propionate 0.05% / niacinamide 4% cream
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-2087 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FLUTICASONE PROPIONATE (UNII: O2GMZ0LF5W) (FLUTICASONE - UNII:CUT2W21N7U) FLUTICASONE PROPIONATE 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:72934-2087-2 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/14/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/14/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-2087)