VETI-FOAM- benzethonium chloride liquid

Veti-Foam by

Drug Labeling and Warnings

Veti-Foam by is a Otc medication manufactured, distributed, or labeled by MWI/Vet One, Continental Manufacturing Chemist, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient(s)

 Benzethonium Chloride 0.20%

Purpose

Use(s)

 for hand washing to decrease bacteria on skin

Warnings

For external use only

Do not use

Ask a doctor before use if

Ask a doctor or pharmacist before use if

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 

Pregnancy/Breastfeeding

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.

Other information

Storage

Inactive ingredients

 Aloe barbadensis (Aloe Vera) Leaf Juice, Ammonium lauryl Sulfate, Cocamidoprpyl Betaine, DMDM Hydantoin, FD&C Blue #1, Fragrance, Glycerin, Purified Water, EDTA

Questions

Principal Display Panel

16oz label

INGREDIENTS AND APPEARANCE

VETI-FOAM 
benzethonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 13985-529
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	2.0 g  in 1.0 L

Inactive Ingredients
Ingredient Name	Strength
EDETATE SODIUM (UNII: MP1J8420LU)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DMDM HYDANTOIN (UNII: BYR0546TOW)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Product Characteristics
Color	BLUE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 13985-529-16	0.473 L in 1 BOTTLE, PUMP
2	NDC: 13985-529-01	3.785 L in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	07/26/2010

Labeler - MWI/Vet One (019926120)

Registrant - Continental Manufacturing Chemist, Inc. (005278007)