HYDROQUINONE 8% EMULSION [SINCERUS FLORIDA, LLC]

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HYDROQUINONE 8% EMULSION [SINCERUS FLORIDA, LLC]
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NDC 72934-6121-2
Set ID 874c1900-82ec-4082-e053-2995a90aff22
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, LLC adverse reactions.

    x

  • Active, inactive

    s

  • NDC 72934-6121-2 Hydroquinone USP 8%. Emulsion 30gm

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  • INGREDIENTS AND APPEARANCE
    HYDROQUINONE 8% 
    hydroquinone 8% emulsion
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-6121
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE8 g  in 100 g
    Product Characteristics
    Coloryellow (BEIGE OPAQUE) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72934-6121-230 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/01/2019
    Labeler - Sincerus Florida, LLC (080105003)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sincerus Florida, LLC080105003manufacture(72934-6121)
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