Label: NIACINAMIDE 4% / SODIUM SULFACETAMIDE MONOHYDRATE 10% cream
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-2156-2 - 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 May 22, 2019
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- Directions for use
- Sincerus Florida, LLC. Adverse reactions
- Active, inactive
- NDC 72934- 2156-2 NIACINAMIDE USP 4% / SODIUM SULFACETAMIDE MONOHYDRATE USP 10%. Cream 30 gm
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INGREDIENTS AND APPEARANCE
NIACINAMIDE 4% / SODIUM SULFACETAMIDE MONOHYDRATE 10%
niacinamide 4% / sodium sulfacetamide monohydrate 10% creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-2156 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFACETAMIDE SODIUM (UNII: 4NRT660KJQ) (SULFACETAMIDE - UNII:4965G3J0F5) SULFACETAMIDE SODIUM 10 g in 100 g NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 4 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-2156-2 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/22/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/22/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-2156)
