Label: HAND SANITIZER COCONUT- alcohol gel

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 12, 2024

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  • ACTIVE INGREDIENTS

    DENATURED DEHYDRATED ALCOHOL 40B  62.5%

  • PURPOSE

    ANTISEPTIC

  • USES

    • For hand washing to decrease bacteria on skin.

  • WARNINGS

    • For external use only. Flammable. Keep away from sources of fire or flame.
    • When using this product do not use near eyes. In case of contact, rinse eyes thoroughly with water.
    • Stop use and ask a doctor if skin irritation develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, seek medical advice or contact a Poison Control Center immediately.

  • DIRECTIONS

    • Apply onto palm of hand.
    • Cover hands with product by thoroughly rubbing and allow to air dry without wiping.
    • Use undiluted.
    • Supervise children under 6 years
    • Not recommended for infants
  • OTHER INFORMATION

    • Store below 86°F / 30°C
    • Keep out of direct sunlight.
  • INACTIVE INGREDIENTS

    WATER, GLYCERIN, PROPYLENE GLYCOL, CARBOMER, PROPANEDIOL, AMINOMETHYL PROPANOL, ALOE BARBADENSIS LEAF JUICE, TOCOPHERYL ACETATE (VITAMIN E ACETATE), HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, VACCINIUM MACROCARPON (CRANBERRY) FRUIT EXTRACT, PUNICA GRANATUM EXTRACT, VACCINIUM ANGUSTOFOLIA (BLUEBERRY) EXTRACT, FRAGARIA VESCA (STRAWBERRY) FRUIT EXTRACT, ACTINIDIA CHINENSIS (KIWI) EXTRACT

  • PRINCIPAL DISPLAY PANEL

    01b LBL_Hand Sanitizer_Coconut_2oz

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER  COCONUT
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73088-204
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    CRANBERRY (UNII: 0MVO31Q3QS)  
    POMEGRANATE (UNII: 56687D1Z4D)  
    BLUEBERRY (UNII: 253RUG1X1A)  
    STRAWBERRY (UNII: 4J2TY8Y81V)  
    KIWI FRUIT (UNII: 71ES77LGJC)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73088-204-1159 mL in 1 BOTTLE; Type 0: Not a Combination Product04/20/202112/30/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00404/20/202112/30/2021
    Labeler - TUBBY TODD (052545299)
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