HYDROQUINONE 6% /TRETINOIN 0.05% emulsion

HYDROQUINONE 6% /TRETINOIN 0.05% by

Drug Labeling and Warnings

HYDROQUINONE 6% /TRETINOIN 0.05% by is a Prescription medication manufactured, distributed, or labeled by Sincerus Florida, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Directions for use

Sincerus Florida, LLC adverse reactions.

Active, inactive

NDC:

72934-6119-2 HYDROQUINONE 6% /TRETINOIN 0.05% Emulsion 30gm.

INGREDIENTS AND APPEARANCE

HYDROQUINONE 6% /TRETINOIN 0.05% 
hydroquinone 6% /tretinoin 0.05% emulsion

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 72934-6119
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)	HYDROQUINONE	6 g  in 100 g
TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R)	TRETINOIN	0.05 g  in 100 g

Product Characteristics
Color	yellow	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72934-6119-2	30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/20/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/20/2019

Labeler - Sincerus Florida, LLC (080105003)

Establishment
Name	Address	ID/FEI	Business Operations
Sincerus Florida, LLC		080105003	manufacture(72934-6119)