REFRESH ANTIBAC FOAM- benzalkonium chloride soap

Refresh AntiBac FOAM by

Drug Labeling and Warnings

Refresh AntiBac FOAM by is a Otc medication manufactured, distributed, or labeled by SC Johnson Professional USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

BENZALKONIUM CHLORIDE, 0.13%

Purpose

Antimicrobial

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

SCJ Professional

A family company
Refresh

ANTIBAC FOAM
EN Citrus Scent Antimicrobial Foam Handwash
ES Jabón antimicrobiano en espuma, aroma cítrico

SC Johnson Professional
Charlotte, NC 28217
1-800-248-7190
www.scjp.com
Made in USA

CITRUS FRAGRANCE

1 L

(33.8 fl oz)

deb

SKIN CARE

1000002413/0219

INGREDIENTS AND APPEARANCE

REFRESH ANTIBAC FOAM 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 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: 11084-010-40	0.4 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/12/2017
2	NDC: 11084-010-27	1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/12/2017
3	NDC: 11084-010-12	1.2 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/12/2017
4	NDC: 11084-010-20	2 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/12/2017
5	NDC: 11084-010-05	3.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/12/2017
6	NDC: 11084-010-01	0.047 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/27/2019
7	NDC: 11084-010-55	208.2 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product	02/27/2019
8	NDC: 11084-010-96	0.296 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2019

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

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

Establishment
Name	Address	ID/FEI	Business Operations
SC Johnson Professional USA, Inc.		078805627	manufacture(11084-010)