Label: BAKUMOKON 5% MINOXIDIL- minoxidil, dutasteride, oxytocin liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated February 9, 2015

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  • INGREDIENTS AND APPEARANCE
    BAKUMOKON 5% MINOXIDIL 
    minoxidil, dutasteride, oxytocin liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:58798-001
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 5 mg  in 100 mg
    DUTASTERIDE (UNII: O0J6XJN02I) (DUTASTERIDE - UNII:O0J6XJN02I) DUTASTERIDE 0.1 mg  in 100 mg
    OXYTOCIN (UNII: 1JQS135EYN) (OXYTOCIN - UNII:1JQS135EYN) OXYTOCIN 0.01 mg  in 100 mg
    Inactive Ingredients
    Ingredient Name Strength
    alcohol (UNII: 3K9958V90M)  
    menthol (UNII: L7T10EIP3A)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    BLACK PEPPER OIL (UNII: U17J84S19Z)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:58798-001-05 12 in 1 DOSE PACK 02/09/2015
    1 5 mg in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    export only 02/09/2015
    Labeler - DS LABORATORIES, INC. (018166259)
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