Label: WELKIN HAND SANITIZER- alcohol gel

  • NDC Code(s): 74979-003-01
  • Packager: Robert Gordon Ind. Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 9, 2024

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active ingredient

    Ethyl alcohol 70% (v/v)

    Purpose

    Antiseptic

  • Uses

    • to decrease bacteria on the skin that could cause disease
    • recommended for repeated use
  • Warnings

    • For external use only
    • Flammable
    • Keep away from fire or flame

    Do not use

    • on children less than 2 months old
    • on open skin wounds

    When using this product

    • keep out of eyes, ears, In case of contact with eyes, flush thoroughly with water.
    • avoid contact with broken skin
    • do not inhale or ingest

    Stop use and ask a doctor if

    • irritation or redness develops
    • 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

    • Place enough product on hands to cover all surfaces.
    • Rub hands together until dry
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    • Do not store above 105°F
    • May discolor some fabrics
    • Harmful to wood finishes and plastics
  • Inactive ingredients

    aminomethyl propanol, carbomer homopolymer, glycerin, propylene glycol, purified water USP

  • Package Labeling:

    Bottle

  • INGREDIENTS AND APPEARANCE
    WELKIN HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74979-003
    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
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74979-003-012 mL in 1 PACKET; Type 0: Not a Combination Product08/21/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/21/2020
    Labeler - Robert Gordon Ind. Ltd. (070064709)