Label: CLETINA HAIR OIL- minoxidil liquid

  • NDC Code(s): 83566-166-01
  • Packager: Guangdong Aimu Biological Technology Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 11, 2024

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  • Active ingredients

    PROPYLENE GLYCOL 10%
    BUTYLENE GLYCOL 5%
    MINOXIDIL 5%

  • Purpose

    Hair growth

  • Uses

    apply half a capful 2 times a day to the scalp in the hair loss area
    massage into scalp with fingers, then wash hands well

  • Warning

    For external use only.

  • Stop use and ask a doctor if

    rash occurs.

  • Do not use

    on damaged or broken skin.

  • When using this product

    keep out of eyes. Rinse withwater to remove.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Dosage

    apply half a capful 2 times a day to the scalp in the hair loss area

  • inactive ingredient

    WATER 46.5599%
    ALCOHOL 33%
    PHENOXYETHANOL 0.3%
    ETHYLHEXYLGLYCERIN 0.1%
    DISODIUM EDTA 0.02%

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CLETINA HAIR OIL 
    minoxidil liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83566-166
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL10 g  in 100 mL
    MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL5 g  in 100 mL
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA) (BUTYLENE GLYCOL - UNII:3XUS85K0RA) BUTYLENE GLYCOL5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83566-166-01120 mL in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)06/12/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03206/12/2024
    Labeler - Guangdong Aimu Biological Technology Co., Ltd (712647107)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Aimu Biological Technology Co., Ltd712647107manufacture(83566-166)
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