ANTIBACTERIAL FOAM- benzalkonium chloride solution

Antibacterial Foam by

Drug Labeling and Warnings

Antibacterial Foam by is a Otc medication manufactured, distributed, or labeled by SC Johnson Professional USA, Inc., APEX International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

BENZALKONIUM CHLORIDE, 0.13%

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.

Stop use and ask a doctor if

irritation and redness develop and persist for more than 3 days.

Keep out of reach of children.

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

Directions

apply foaming cleanser to dry hands
rub hands together to spread lather
wash for 15-20 seconds
rinse & dry hands thoroughly

Inactive ingredients

AQUA (WATER), GLYCERIN, LAURAMINE OXIDE, BUTYLENE GLYCOL, LACTIC ACID, SALICYLIC ACID, PARFUM (FRAGRANCE), GREEN 5 (CI 61570), YELLOW 5 (CI 19140).

PRINCIPAL DISPLAY PANEL

This product does not contain any prop65 ingredients.

TSFG1

DCN9290

TOTO

Antibacterial Foam Soap

Cleans hands!

Kills germs!

Moisturizes!

Triclosan-free!

One Gallon (3.78 Liters)

Product Features

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

This product contains moisturizers and emollients for the skin making it ideal for frequent use environments.

Manufactured for:

TOTO USA, Inc.

1155 Southern Road

Morrow, GA 30260

888-295-8134

Made in the USA

R00

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL FOAM 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-021
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
LACTIC ACID (UNII: 33X04XA5AT)
SALICYLIC ACID (UNII: O414PZ4LPZ)
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: 11084-021-05	3.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2017
2	NDC: 11084-021-42	18.93 L in 1 PAIL; Type 0: Not a Combination Product	08/01/2017
3	NDC: 11084-021-55	208.20 L in 1 DRUM; Type 0: Not a Combination Product	08/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/01/2017

Labeler - Deb USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
Deb USA, Inc.		078805627	manufacture(11084-021)