Label: GENUINE FIRST AID HAND SANITIZER ETHYL ALCOHOL- alcohol gel

  • NDC Code(s): 50814-063-01, 50814-063-02
  • Packager: GFA Production (Xiamen) Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated October 25, 2023

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  • Drug Facts

  • Active ingredient

    Ethyl alcohol 70% v/v

    Purpose

    Antiseptic

  • Uses

    • For hand washing to decrease bacteria on the skin that may cause disease.
    • Recommended for repeated use. 
  • Warnings

    Flammable, keep away from fire or flame 

    For external use only.

    Intended for use exclusively by adults.

    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 todry without wiping.
  • Other information

    Store at 15° to 25°C (59° to 77°F)

  • Inactive ingredients

    Acrylic acid Polymers, Propylene glycol, Trolamine, Purified water.

  • Package Labeling:473ml

    Bottle

  • Package Labeling:946ml

    Bottle7

  • INGREDIENTS AND APPEARANCE
    GENUINE FIRST AID HAND SANITIZER ETHYL ALCOHOL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50814-063
    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
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50814-063-01473 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
    2NDC:50814-063-02946 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 Drug505G(a)(3)08/01/2020
    Labeler - GFA Production (Xiamen) Co., Ltd. (421256261)