ANTIBAC FOAM WASH- triclosan liquid
Deb USA, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

Triclosan, 0.30%

Purpose

Antibacterial

Uses

For handwashing to reduce bacteria on the skin

Warnings

For external use only

When using this product avoid contact with eyes.

In case of eye contact, flush with water.

Keep out of reach of children.

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

Directions

Apply foam cleanser to dry hands.

Rub hands together to spread lather

Wash for 15-20 seconds

Rinse and dry hands thoroughly

Inactive ingredients

Water, Sodium Laureth Sulfate, Propylene Glycol, PPG-24-Glycereth-24, Cocamidopropyl Betaine, Tetrasodium EDTA, 2-bromo-2-nitropropane-1,3-diol, Fragrance, Citric Acid, Green 5 (CI 61570), Yellow 5 (CI 19140)

deb

AntiBac Foam Wash

Antibacterial Foaming Hand Soap

A high-quality, foam soap that is 99.99% effective against common bacteria.

Ideal for...

General Industry

Healthcare

Schools

Manufacturing

Office Environments

Made in USA

Deb, Stanley, NC 28164

1-800-248-7190

www.debgroup.com

ANT400ML

13.5 fl. oz. (400 mL)

Rev. 09-11

container label

ANTIBAC FOAM WASH
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11084-125
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.30 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:11084-125-40	400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2011	10/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	10/01/2011	10/01/2016

Labeler - Deb USA, Inc. (607378015)

Name	Address	ID/FEI	Business Operations
Establishment
Deb USA, Inc.		078805627	manufacture(11084-125)

Revised: 11/2017

Document Id: f922cc7b-6463-4b5e-8586-c006dfda8113

Set id: 4b2b3047-d9bb-4d01-b245-66517464db2e

Version: 9

Effective Time: 20171106

Deb USA, Inc.