Label: CLOBETASOL PROPIONATE 0.05% / NIACINAMIDE 4% cream
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-2059-3 - 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 April 30, 2019
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- Official Label (Printer Friendly)
- Directions for use
- Sincerus Florida, LLC adverse reactions.
- Active, inactive
- NDC 72934-2059-3 CLOBETASOL PROPIONATE 0.05% / NIACINAMIDE 4%. Cream 60gm
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INGREDIENTS AND APPEARANCE
CLOBETASOL PROPIONATE 0.05% / NIACINAMIDE 4%
clobetasol propionate 0.05% / niacinamide 4% creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-2059 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLOBETASOL PROPIONATE (UNII: 779619577M) (CLOBETASOL - UNII:ADN79D536H) CLOBETASOL 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:72934-2059-3 60 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/01/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-2059)
