Allantoin .4%: Product Information

ALLANTOIN .4%- allantoin liquid
avadim II, LLC

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.

Alcohol Free Spray

VetraCare Pet Liquid Bandage

2 fl oz (60ml)

(click image for full-size original)


LB2.jpg LB2

Active ingredient Allantoin .8% Skin Protectant


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


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


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

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 DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Allantoin (ALLANTOIN) Allantoin 4 g in 1000 mL
Inactive Ingredients
Ingredient Name Strength
ALOE 1 g in 1000 mL
water 950 mL in 1000 mL
silicon 3 g in 1000 mL
# Item Code Package Description Multilevel Packaging
1 NDC:51098-501-01 60 mL in 1 BOTTLE, SPRAY None
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)
Name Address ID/FEI Operations
avadim II, LLC 962520412 manufacture

Revised: 10/2013 avadim II, LLC provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the U.S. Food and Drug Administration. Package information is not reviewed or updated separately by Every individual animal healthcare product label entry contains a unique identifier which can be used to secure further details directly from the U.S. National Institutes of Health and/or the FDA.

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