IMIQUIMOD 5% / SALICYLIC ACID 30% / TRETINOIN 0.1%- imiquimod 5% / salicylic acid 30% / tretinoin 0.1% gel 
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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IMIQUIMOD 5% / SALICYLIC ACID 30% / TRETINOIN 0.1%

Directions for use

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Sincerus Florida. Adverse reactions

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Active, inactive

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NDC 72934-1128-2 IMIQUIMOD USP 5% / SALICILIC ACID USP 30%/ TRETINOIN USP 0.1%. Gel 30 gm.

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IMIQUIMOD 5% / SALICYLIC ACID 30% / TRETINOIN 0.1% 
imiquimod 5% / salicylic acid 30% / tretinoin 0.1% gel
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-1128
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID30 g  in 100 g
TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN0.1 g  in 100 g
IMIQUIMOD (UNII: P1QW714R7M) (IMIQUIMOD - UNII:P1QW714R7M) IMIQUIMOD5 g  in 100 g
Product Characteristics
ColoryellowScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72934-1128-230 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/07/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/07/2019
Labeler - Sincerus Florida, LLC (080105003)
Establishment
NameAddressID/FEIBusiness Operations
Sincerus Florida, LLC080105003manufacture(72934-1128)

Revised: 5/2019
Document Id: 883a24d3-e5fe-4329-e053-2995a90a9758
Set id: 883a24d3-e5fd-4329-e053-2995a90a9758
Version: 1
Effective Time: 20190506
 
Sincerus Florida, LLC