NIACINAMIDE 4% / SODIUM SULFACETAMIDE MONOHYDRATE 10% / SULFUR PRECIPITATED 2%- niacinamide 4% / sodium sulfacetamide monohydrate 10% / sulfur precipitated 2% cream
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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NIACINAMIDE 4% / SODIUM SULFACETAMIDE MONOHYDRATE 10% / SULFUR PRECIPITATED 2%

Directions for use

Sinceus Florida, LLC. Adverse reactions

zsd

Active, inactive

NDC 72934- 2155-2 NIACINAMIDE 4% / SODIUM SULFACETAMIDE MONOHYDRATE 10% / SULFUR PRECIPITATED 2%. Cream 30gm.

NIACINAMIDE 4% / SODIUM SULFACETAMIDE MONOHYDRATE 10% / SULFUR PRECIPITATED 2%
niacinamide 4% / sodium sulfacetamide monohydrate 10% / sulfur precipitated 2% cream

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:72934-2155
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72934-2155-2	30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/15/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		05/15/2019

Labeler - Sincerus Florida, LLC (080105003)

Name	Address	ID/FEI	Business Operations
Establishment
Sincerus Florida, LLC		080105003	manufacture(72934-2155)