Label: SOLUCION CAPILAR CRECEPELO- minoxidil liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 24, 2024

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

  • DOSAGE & ADMINISTRATION

    DOSAGE AND ADMINISTRATION

    take only as directed

  • WARNINGS

    SKIN: Here are no known effects on contact with Skin, in case of irritation, rinse with water for a few minutes. Get medical attention if Irritation persists. INGESTION: Drink plenty of water and consult your doctor.

  • INACTIVE INGREDIENT

    WATER PURIFIED S.C.P. ETHYIL ALCOHOL 30 PROPYLENGLYCOL 25 LACTIC ACID 1.0 TRITICUM VULGARE GLYCINE SOJA/EXCTRAT 0.5 FRAGRANCE 0.02 TETRASODIUM EDTA

  • INDICATIONS & USAGE

    use as directed

  • KEEP OUT OF REACH OF CHILDREN

    If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms

  • PURPOSE

    Uses

    HAIR REGROWTH TREATMENT

  • ACTIVE INGREDIENT

    MINOXIDIL 5%

  • PRINCIPAL DISPLAY PANEL

    12

  • INGREDIENTS AND APPEARANCE
    SOLUCION CAPILAR CRECEPELO 
    minoxidil liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78192-400
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL5 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    LACTIC ACID (UNII: 33X04XA5AT) 1 mL  in 30 mL
    EDETATE SODIUM (UNII: MP1J8420LU) 0.02 mL  in 30 mL
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 25 mL  in 30 mL
    WHEAT SPROUT (UNII: 3K32950CI0) 0.5 mL  in 30 mL
    FRAGRANCE 13576 (UNII: 5EM498GW35) 0.02 mL  in 30 mL
    ALCOHOL (UNII: 3K9958V90M) 30 mL  in 30 mL
    WATER (UNII: 059QF0KO0R) 1 mL  in 30 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78192-400-01123 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product06/25/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/25/2024
    Labeler - BOE Dominicana SRL (871487430)
    Establishment
    NameAddressID/FEIBusiness Operations
    BOE Dominicana SRL871487430label(78192-400) , manufacture(78192-400)