BENZOYL PEROXIDE 8% / NIACINAMIDE 4% suspension

BENZOYL PEROXIDE 8% / NIACINAMIDE 4% by

Drug Labeling and Warnings

BENZOYL PEROXIDE 8% / NIACINAMIDE 4% by is a Prescription medication manufactured, distributed, or labeled by Sincerus Florida, Sincerus Florida, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Directions for use

Sincerus Florida, LLC. Adverse reactions

Active, inactive

NDC:

72934-8022-6 BENZOYL PEROXIDE USP 8% / NIACINAMIDE USP 4%. Suspension 120gm.

INGREDIENTS AND APPEARANCE

BENZOYL PEROXIDE 8% / NIACINAMIDE 4% 
benzoyl peroxide 8% / niacinamide 4% suspension

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 72934-8022
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM)	BENZOYL PEROXIDE	8 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: 72934-8022-6	120 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/11/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/11/2019

Labeler - Sincerus Florida (080105003)

Establishment
Name	Address	ID/FEI	Business Operations
Sincerus Florida, LLC		080105003	manufacture(72934-8022)