FROSTY GREEN ANTIBACTERIAL FOAM HAND- 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, PARFUM (FRAGRANCE), GREEN 5 (CI 61570), YELLOW 5 (CI 19140).

57258-DCN9286 FrostyGreen 1L- V7.jpg

Frosty Green

ANTIBACTERIAL FOAM HAND SOAP

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

PIONEER CHEMICAL COMPANY(TM)

Manufactured for:

PIONEER CHEMICAL

13717 S. Normandie Avenue

Gardena, CA 90249

1-800-824-5492

www.pioneerchem.com

57258 DCN9286

1 Liter (33.8 fl oz)

FROSTY GREEN ANTIBACTERIAL FOAM HAND
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11084-019
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)
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:11084-019-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/12/2017	02/28/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	06/12/2017	02/28/2023

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

Name	Address	ID/FEI	Business Operations
Establishment
SC Johnson Professional USA, Inc.		078805627	manufacture(11084-019)

Revised: 11/2020

Document Id: f0dd3553-3ce5-41ed-b690-7bbb2093f10d

Set id: 9eb10c0c-ddbc-45c1-9fc4-7faf5c32f57d

Version: 2

Effective Time: 20201125

SC Johnson Professional USA, Inc.