Label: COBRA CLEAN HANDS- isopropyl alcohol 75% spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated October 20, 2020

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  • Active Ingredient

    Isopropyl Alcohol 75%

  • Purpose

    Antiseptic

  • Uses

    Helps reduce the spread of germs
    Recommended for repeat us as needed

  • Warnings

    For External Use only
    Flammable, keep away from fire, sparks, and source of ignition
    Do not store above 104 F/40C

  • Do not Use

    with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist
    if you have ever had an allergic reaction to this product or any of its ingredients

  • When using this product

    Keep out of eyes
    In case of contract with eyes, flush with water
    avoid contact with broken skin
    Do not inhale or ingest

  • Stop use and ask a doctor if

    irritation develops

  • Keep out of reach of children

    If swallowed seek medical attention or call Center for Poison Control Center

  • Directions

    Spray on hands and rub all over
    Use adult supervision for children
    Not recommended for babies

  • Inactive Ingredients

    Water, Aloe Barbadensis (leaf), Fragrance, Glycerin

  • Cobra Clean Hands

    label

  • INGREDIENTS AND APPEARANCE
    COBRA CLEAN HANDS 
    isopropyl alcohol 75% spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73761-103
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL45 mL  in 60 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73761-103-6060 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A10/01/2020
    Labeler - Nutralife Biosciences, Inc. (078834338)
    Registrant - Nutralife Biosciences, Inc. (078834338)
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