IVERMECTIN 1% / METRONIDAZOLE 1% GEL [SINCERUS FLORIDA, LLC]

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  • IVERMECTIN 1% / METRONIDAZOLE 1% GEL [SINCERUS FLORIDA, LLC]

IVERMECTIN 1% / METRONIDAZOLE 1% GEL [SINCERUS FLORIDA, LLC]
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NDC 72934-1130-2
Set ID 874c79d7-7766-3d66-e053-2995a90a6d5c
Category HUMAN PRESCRIPTION DRUG LABEL
Packager Sincerus Florida, LLC
Generic Name
Product Class Antiparasitic
Product Number
Application Number
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  • Directions for use

    x

  • Sincerus Florida, LLC adverse reactions.

    p

  • Active, Inactive

    h

  • NDC 72934-1130-2 IVERMECTIN USP 1% / METRONIDAZOLE USP 1% gel 30 gm

    c

  • INGREDIENTS AND APPEARANCE
    IVERMECTIN 1% / METRONIDAZOLE 1% 
    ivermectin 1% / metronidazole 1% gel
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-1130
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    METRONIDAZOLE (UNII: 140QMO216E) (METRONIDAZOLE - UNII:140QMO216E) METRONIDAZOLE1 g  in 100 g
    IVERMECTIN (UNII: 8883YP2R6D) (IVERMECTIN - UNII:8883YP2R6D) IVERMECTIN1 g  in 100 g
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72934-1130-230 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(72934-1130)
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