Label: HAND-AID- alcohol gel

  • NDC Code(s): 62257-122-01, 62257-122-13, 62257-122-14, 62257-122-17, view more
    62257-122-21, 62257-122-24, 62257-122-28, 62257-122-47, 62257-122-55
  • Packager: ABC Compounding Co., Inc.
  • 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 January 15, 2021

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Drug Facts Box OTC-Active Ingredient Section

    Ethyl Alcohol 70% v/v

  • Drug Facts Box OTC-Purpose Section

    Antiseptic

  • Drug Facts Box OTC-Indications & Usage Section

    for hand-washing to decrease bacteria on the skin, only when water is not available

  • Drug Facts Box OTC-Warnings Section

    FLAMMABLE, keep away from fire and flames

    For external use only

  • Drug Facts Box OTC-When Using Section

    do not get into eyes

    if contact occurs, rinse eyes thoroughly with water

  • Drug Facts Box OTC-Stop Use Section

    irritation and redness develop

  • Drug Facts Box OTC-Keep Out of Reach of Children Section

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

  • Drug Facts Box OTC-Dosage & Administration Section

    wet hands thoroughly with product and allow to dry without wiping

  • Drug Facts Box OTC-Inactive Ingredient Section

    water, DMDM hydantoin, diidopropylamine, carbomer, propylene glycol, tocopheryl acetate, aloe barbadensis, 

  • Hand-Aid 6605 Drug Facts and Label

    product label6605M4PA_Hand-Aid 800ml bag 1-15-2021

  • INGREDIENTS AND APPEARANCE
    HAND-AID 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62257-122
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER 934 (UNII: Z135WT9208)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    DIISOPROPYLAMINE (UNII: BR9JLI40NO)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62257-122-17532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/15/2021
    2NDC:62257-122-24118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/15/2021
    3NDC:62257-122-011200 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/15/2021
    4NDC:62257-122-28149 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/15/2021
    5NDC:62257-122-143785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/15/2021
    6NDC:62257-122-13800 mL in 1 BAG; Type 0: Not a Combination Product01/15/2021
    7NDC:62257-122-47473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/15/2021
    8NDC:62257-122-17532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/15/2021
    9NDC:62257-122-55208200 mL in 1 DRUM; Type 0: Not a Combination Product01/15/2021
    10NDC:62257-122-212.5 mL in 1 DOSE PACK; Type 0: Not a Combination Product01/15/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/15/2021
    Labeler - ABC Compounding Co., Inc. (003284353)
    Registrant - ABC Compounding Co., Inc. (003284353)
    Establishment
    NameAddressID/FEIBusiness Operations
    ABC Compounding Co., Inc.003284353manufacture(62257-122)