Label: 141067 HYDROQUINONE 8% emulsion

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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.

Drug Label Information

Updated July 2, 2020

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  • Directions for use

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  • Sinceus Florida, LLC adverse reactions

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  • Active, inactive

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  • NDC 72934-6234-2 141067 HYDROQUINONE 8% Emulsion 30 gm

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  • INGREDIENTS AND APPEARANCE
    141067 HYDROQUINONE 8% 
    141067 hydroquinone 8% emulsion
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-6234
    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) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72934-6234-230 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/02/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/02/2020
    Labeler - Sincerus Florida, LLC (080105003)
    Registrant - Sincerus Florida, LLC (080105003)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sincerus Florida, LLC080105003manufacture(72934-6234)