IMIQUIMOD 5% / TRETINOIN 0.025% GEL [SINCERUS FLORIDA, LLC]

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  • IMIQUIMOD 5% / TRETINOIN 0.025% GEL [SINCERUS FLORIDA, LLC]

IMIQUIMOD 5% / TRETINOIN 0.025% GEL [SINCERUS FLORIDA, LLC]
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NDC 72934-1129-2
Set ID 8839ed49-b52a-11f6-e053-2a95a90a7492
Category HUMAN PRESCRIPTION DRUG LABEL
Packager Sincerus Florida, LLC
Generic Name
Product Class
Product Number
Application Number
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  • Directions for use

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  • Sincerus Florida. Adverse reactions

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  • Active, inactive

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

    ca

  • INGREDIENTS AND APPEARANCE
    IMIQUIMOD 5% / TRETINOIN 0.025% 
    imiquimod 5% / tretinoin 0.025% gel
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-1129
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN0.025 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:72934-1129-230 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 Floida, LLC080105003manufacture(72934-1129)
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