Label: RAPHE PHARMACEUTIQUE- minoxil aerosol, foam

  • NDC Code(s): 82627-005-01, 82627-005-02
  • Packager: Amwiner & Raphe Holdings LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated August 30, 2023

If you are a consumer or patient please visit this version.

  • EXTRA STRENGTH MINOXIDIL HAIR FOAM FOR MEN & WOMEN

    60ml NDC 82627-00260ml NDC 82627-005-01EXTRA STRENGTH MINOXIDIL HAIR FOAM FOR MEN & WOMEN

    Active Ingredient: Minoxidil Sulfate 5%W/V

    Purpose: Anti-Hair Loss

    Uses: Helps Reactivate Hair Follicles, And Increase Hair Volume And Density

    Helps Eliminate Recurrence of Hair Loss.

    Warnings:

    For external use only

    Ask a doctor before use if condition covers a large area.

    When using this product avoid contact with the eyes. If contact occurs, rinse your eyes thoroughly with water.

    Stop use and ask a doctor if condition worsens or does not improve after regular use of the product as directed.

    Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center right away.

    Directions

    Apply to affected area one ml two times daily or as directed by the physician!

    Inactive Ingredients: Water, Cocoamidopropylbetaine, Green Tea, Extract,Hyaluronic Acid, Biotin, Ginseng Panax, Keratin Amino Acid, Melatonin, Ketoconazole, Menthol

    Other information

    Store at 59° to 77°F (15° to 25°C)

    For Questions Call 1-469-428-5508

  • INGREDIENTS AND APPEARANCE
    RAPHE PHARMACEUTIQUE 
    minoxil aerosol, foam
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82627-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL50 mg  in 50 mg
    Product Characteristics
    Colorbrown (Light amber foamy liquid) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82627-005-021 in 1 BOX09/01/2023
    1NDC:82627-005-0150 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Export only08/31/2023
    Labeler - Amwiner & Raphe Holdings LLC (113433590)
    Establishment
    NameAddressID/FEIBusiness Operations
    AmWiner & Raphe Holdings Llc113433590manufacture(82627-005)