BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% SOLUTION [SINCERUS FLORIDA, LLC]

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BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% SOLUTION [SINCERUS FLORIDA, LLC]
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NDC 72934-4023-8
Set ID 8747c1ea-6b24-46c8-e053-2995a90a33df
Category HUMAN PRESCRIPTION DRUG LABEL
Packager Sincerus Florida, LLC
Generic Name
Product Class Arteriolar Vasodilator
Product Number
Application Number
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  • Directions for use

    e

  • Sincerus Florida, LLC adverse reactions.

    z

  • Active, inactive

    x

  • NDC 72934-4023-8 BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% Solution 60gm

    x

  • INGREDIENTS AND APPEARANCE
    BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% 
    betamethasone dipropionate 0.05% / minoxidil 5% solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-4023
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL5 g  in 100 g
    BETAMETHASONE DIPROPIONATE (UNII: 826Y60901U) (BETAMETHASONE - UNII:9842X06Q6M) BETAMETHASONE0.05 g  in 100 g
    Product Characteristics
    Colorwhite (CLEAR SOLUTION) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72934-4023-860 g in 1 BOTTLE, GLASS; 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(72934-4023)
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