Label: HANDY ANTIBAC ANTISEPTIC INSTANT GEL HAND SANITIZER- alcohol gel

  • Category: HUMAN OTC DRUG LABEL

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 8, 2021

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  • Drug Facts

  • Active ingredient

    Ethyl alcohol 65%

    Purpose

    Antiseptic

  • Use

    For hand washing to decrease bacteria on the skin

  • Warnings

    For external use only Flammable, keep away from fire or flame.

    Do not use

    in the eyes.

    Stop use and ask a doctor if

    • irritation and redness develop 
    • condition persists for more than 72 hours

    Keep out of reach of children.

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

  • Directions

    wet hands thoroughly with product and allow to dry without wiping

  • Other information

    • Do not store above 104°F (40°C) 
    • May discolor some fabrics or surfaces
  • Inactive ingredients

    Water, glycerol, aloe vera leaf juice, carbomer, triethanolamine.

  • Package Labeling:30ml

    Label

  • Package Labeling:60ml

    Label2

  • Package Labeling:500ml

    Label3

  • Package Labeling:1000ml

    Label4

  • INGREDIENTS AND APPEARANCE
    HANDY ANTIBAC ANTISEPTIC INSTANT GEL HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79873-000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.65 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79873-000-0030 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
    2NDC:79873-000-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
    3NDC:79873-000-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/202010/08/2021
    4NDC:79873-000-031000 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/202010/08/2021
    5NDC:79873-000-04500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/01/2020
    6NDC:79873-000-051000 mL in 1 POUCH; 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 - Lentus LLC (078554629)
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