Label: HEALTH SMART HAND SANITIZER PEACH- alcohol gel

  • NDC Code(s): 52862-610-08
  • Packager: International Wholesale Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 14, 2023

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  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 62%

    Purpose

    Antimicrobial

  • Uses

    • helps reduce bacteria on the skin that could cause disease.
    • Recommended for repeated use
  • Warnings

    For external use only.

    Flammable.Keep away from fire or flame.

    When using this product:

    do not use in or near the eyes. In case of eye contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if:

    irritation and redness develops and lasts more than 72 hours.

    Keep out of reach of children.

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

  • Directions

    • Place enough product in your palm to thoroughly cover your hands
    • Rub hands together briskly until dry
    • Children under 6 years of age should be supervised when using this product.
  • Other Information:

    • Store below 110°F(43°C)
    • May discolor certain fabrics or surfaces
  • Inactive Ingredients:

    Water, Aloe Barbadensis Gel, Carbomer, Glycerin, Triethanolamine, Tocopheryl Acetate, FD&C Red No 40, FD&C Yellow No.5

  • Package Labeling

    Label5

  • INGREDIENTS AND APPEARANCE
    HEALTH SMART HAND SANITIZER PEACH 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52862-610
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52862-610-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product06/22/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/22/2020
    Labeler - International Wholesale Inc (161872676)
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