SALICYLIC ACID 2% / SODIUM SULFACETAMIDE MONOHYDRATE 8%

SALICYLIC ACID 2% / SODIUM SULFACETAMIDE MONOHYDRATE 8%- sulfacetamide sodium and salicylic acid suspension
Sincerus Florida, LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Sincerus Florida, LLC. Adverse reactions

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NDC 72934- 8171-6 SALICYLIC ACID USP 2% / SODIUM SULFACETAMIDE MONOHYDRATE USP 8%.

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SALICYLIC ACID 2% / SODIUM SULFACETAMIDE MONOHYDRATE 8%
salicylic acid 2% / sodium sulfacetamide monohydrate 8% suspension
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-8171
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SULFACETAMIDE SODIUM (SULFACETAMIDE) SULFACETAMIDE SODIUM 8 g in 100 g
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID 2 g in 100 g
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:72934-8171-6 120 g in 1 CYLINDER None
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 Operations
Sincerus Florida, LLC 080105003 manufacture (72934-8171)

Revised: 05/2019 Sincerus Florida, LLC

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