ANTIBAC FOAM WASH/AEROGREEN- triclosan liquid

AntiBac Foam Wash/Aerogreen by

Drug Labeling and Warnings

AntiBac Foam Wash/Aerogreen by is a Otc medication manufactured, distributed, or labeled by Deb USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Triclosan, 0.30%

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

Uses

For handwashing to reduce bacteria on the skin

WARNINGS

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.

DOSAGE & ADMINISTRATION

Directions

Apply foam cleanser to dry hands.

Rub hands together to spread lather

Wash for 15-20 seconds

Rinse and dry hands thoroughly

INACTIVE INGREDIENT

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)

PRINCIPAL DISPLAY PANEL

deb

AntiBac Foam Wash/AeroGreen

1L

33.8 fl. oz.

Made in USA

Deb USA, Inc.

Charlotte, NC 28217

1-800-248-7190

www.debgroup.com

57250

AntiBacFoamWash

Rev. 04-13

INGREDIENTS AND APPEARANCE

ANTIBAC FOAM WASH/AEROGREEN 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-253
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-253-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2013	08/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2013	08/01/2020

Labeler - Deb USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
Deb USA, Inc.		078805627	manufacture(11084-253)