Label: SALICYLIC ACID 2% / SODIUM SULFACETAMIDE MONOHYDRATE 8% suspension
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-8171-6 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated May 16, 2019
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- Official Label (Printer Friendly)
- Directions for use
- Sincerus Florida, LLC. Adverse reactions
- Active, inactive
- NDC 72934- 8171-6 SALICYLIC ACID USP 2% / SODIUM SULFACETAMIDE MONOHYDRATE USP 8%.
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID 2% / SODIUM SULFACETAMIDE MONOHYDRATE 8%
salicylic acid 2% / sodium sulfacetamide monohydrate 8% suspensionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-8171 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFACETAMIDE SODIUM (UNII: 4NRT660KJQ) (SULFACETAMIDE - UNII:4965G3J0F5) SULFACETAMIDE SODIUM 8 g in 100 g SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-8171-6 120 g in 1 CYLINDER; Type 0: Not a Combination Product 05/17/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/17/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-8171)
