CLEAR FOAMING ANTIMICROBIAL- benzalkonium chloride solution
SC Johnson Professional 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

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

57151-DCN9283 ActionChem-V9.jpg

CLEAR FOAMING ANTIMICROBIAL SOAP

Ideal for use where antimicrobial action is desired.

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

ACTION

JANITORIAL . PAPER . SAFETY

275 Cumberland Street, Memphis, TN 38112

www.actionjps.com

Phone: 901-522-8783

Toll Free Phone: 877-422-8783

57151

1 Liter (33.8 fl oz)

DCN9283

CLEAR FOAMING ANTIMICROBIAL
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11084-016
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
LACTIC ACID (UNII: 33X04XA5AT)
SALICYLIC ACID (UNII: O414PZ4LPZ)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:11084-016-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/12/2017	03/31/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	06/12/2017	03/31/2022

Labeler - SC Johnson Professional USA, Inc. (607378015)

Name	Address	ID/FEI	Business Operations
Establishment
SC Johnson Professional USA, Inc.		078805627	manufacture(11084-016)

Revised: 11/2020

Document Id: 36594899-0716-4691-b572-844930b37b58

Set id: fb4a1753-5f4f-4173-9ddd-22a4d25ce8a4

Version: 2

Effective Time: 20201125

SC Johnson Professional USA, Inc.