IMIQUIMOD 5% / TRETINOIN 0.025% gel

IMIQUIMOD 5% / TRETINOIN 0.025% by

Drug Labeling and Warnings

IMIQUIMOD 5% / TRETINOIN 0.025% by is a Prescription medication manufactured, distributed, or labeled by Sincerus Florida, LLC, Sincerus Floida, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Directions for use

Sincerus Florida. Adverse reactions

Active, inactive

NDC:

72934-1129-2 IMIQUIMOD USP 5% / TRETINOIN USP 0.025%. Gel 30 gm

INGREDIENTS AND APPEARANCE

IMIQUIMOD 5% / TRETINOIN 0.025% 
imiquimod 5% / tretinoin 0.025% gel

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 72934-1129
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R)	TRETINOIN	0.025 g  in 100 g
IMIQUIMOD (UNII: P1QW714R7M) (IMIQUIMOD - UNII:P1QW714R7M)	IMIQUIMOD	5 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: 72934-1129-2	30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/07/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/07/2019

Labeler - Sincerus Florida, LLC (080105003)

Establishment
Name	Address	ID/FEI	Business Operations
Sincerus Floida, LLC		080105003	manufacture(72934-1129)