Label: ALLANTOIN .4%- vetracare pet liquid bandage liquid

  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated October 1, 2013

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  • PRINCIPAL DISPLAY PANEL

    Alcohol Free Spray

    VetraCare Pet Liquid Bandage

    2 fl oz (60ml)LB2

    Image

    LB2.jpg  LB2

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  • VETERINARY INDICATIONS

    Active ingredient Allantoin .8% Skin Protectant

    Uses

    Treat and protect minor cuts, scrapes, and irritations

    waterproof, breathable protection promotes wound healing

    Creates invisible barrier to keep out bacteria and debris

    Alcohol free formula for gentle, no sting protection

    Directions

    Gently clean and dry the wound and surrounding skin

    shake well. Spray onto affected area and allow to air dry

    product will create waterproof barrier once dry

    Apply as often as needed

    Warning

    For external use only

    Keep out of the reach of children

    Do not use in the eyes

    Stop use and ask a vet if condition worsens or symptoms last more than seven days.

    Inactive ingredients

    Purified water, phenochem, aloe vera, polydimethylsiloxane, grapefruit seed extract, EDTA

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  • INGREDIENTS AND APPEARANCE
    ALLANTOIN .4% 
    vetracare pet liquid bandage liquid
    Product Information
    Product Type OTC ANIMAL DRUG Item Code (Source) NDC:51098-501(NDC:51098-742)
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Allantoin (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) Allantoin 4 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALOE (UNII: V5VD430YW9) 1 g  in 1000 mL
    water (UNII: 059QF0KO0R) 950 mL  in 1000 mL
    silicon (UNII: Z4152N8IUI) 3 g  in 1000 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51098-501-01 60 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 10/01/2013
    Labeler - avadim II, LLC (962520412)
    Registrant - Avadim II, LLC (962520412)
    Establishment
    Name Address ID/FEI Business Operations
    avadim II, LLC 962520412 manufacture
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