Label: HAND SANITIZER GLOBAL CARE (ISOPROPYL)- isopropyl alcohol liquid

  • 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 August 10, 2020

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  • Drug Facts

  • Active ingredient

    Isopropyl Alcohol 70%

    Purpose

    Antimicrobial

  • Uses

    hand sanitizer to help reduce bacteria on the skin.

  • Warnings

    For external use only.

    Flammable. Keep away from heat and flame.

    When using this product

    avoid contact with face, eyes, and broken skin. In case of contact, flush with plenty of water and seek medical advice.

    Stop use and ask a doctor if

    irritation or redness develops.

    Keep out of reach of children.

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

  • Directions

    • wet hands thoroughly with product and rub into skin until dry.
    • Children under 6 years of age should be supervised by an adult when using.
  • Inactive ingredients

    Water, Propylen Glycol, Glycerine, Triethanolamine, Carbomer

  • Package Labeling:

    Bottle

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER GLOBAL CARE (ISOPROPYL) 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72146-030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72146-030-013785.41 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/01/2020
    Labeler - TARGET PRICE INC (081086884)
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