KONG HANDIPOD (ALCOHOL) GEL [HANDIPOD LIMITED]

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KONG HANDIPOD (ALCOHOL) GEL [HANDIPOD LIMITED]
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NDC 71427-213-45
Set ID 352993f4-f076-476e-b2e5-b9ff0af5eeec
Category HUMAN OTC DRUG LABEL
Packager HANDIPOD LIMITED
Generic Name
Product Class
Product Number
Application Number PART333E
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  • Drug Facts

  • Active Ingredinet

    Ethanol 70.0% v/v (70.0g/per 100g)

    Purpose

    Antimicrobial

  • Uses

    • Hand sanitizer to help reduce germs on the skin.
  • Warnings

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

    When using this product

    do not use

    in or near the eyes. In case of contact, remove contact lenses if present, rinse thoroughly with water for several minutes. If eye irritation persists: Get medical attention - show this packaging or gel container.

    Stop use and ask a doctor if

    irritation or rash appears and lasts.

    Keep out of reach of children.

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

  • Directions

    • Put enough product in your palm to cover hands and rub hands together briskly until dry, ensuring contact with finger nails and in between fingers. Do not use on damaged, sensitive or irritated skin.
    • Children under 6 years of age should be supervised when using this hand sanitizer.

  • Other Information

    • Store below 110⁰F (43⁰C). Store in a well ventilated place.
    • May discolor certain fabrics or surfaces
    • Keep out of reach of children. If swallowed seek medical advice immediately and show this packaging or gel container.
    • Microbiological Testing: Bactericidal according to: BS EN1500.

  • Inactive ingredients

    Alcohol Denat, Aqua, Carbomer, Glycerin, Aminomethylpropanol, parfum CI 17200, 42090.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    KONG HANDIPOD 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71427-213
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL700 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71427-213-4545 mL in 1 BOTTLE; Type 0: Not a Combination Product05/09/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/09/2017
    Labeler - HANDIPOD LIMITED (220732701)
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