Active Ingredient(S)
Benzethonium Chloride 0.20%
Veti-foam
FDA Label NDC 13985-529
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Mwi/vet One for the product Veti-foam (NDC 13985-529). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient(s), use(s), when using this product, stop use and ask a doctor if, keep out of reach of children, directions, inactive ingredients, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Use(S)
for hand washing to decrease bacteria on skin
When Using This Product
- Avoid contact with eyes; in case of contact, thoroughly rinse eyes with water. Seek medical attention if irritation persists.
Stop Use And Ask A Doctor If
- skin rash or redness develops when using this product
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Use 1-2 pumps of product on plam. Rub lather completely around hands and between fingers. Scrub thoroughly and rinse with water.
Inactive Ingredients
Aloe barbadensis (Aloe Vera) Leaf Juice, Ammonium lauryl Sulfate, Cocamidoprpyl Betaine, DMDM Hydantoin, FD&C Blue #1, Fragrance, Glycerin, Purified Water, EDTA
Principal Display Panel
16oz label
* Please review the disclaimer below.
