REFRESH ANTIBAC FOAM- benzalkonium chloride soap 
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

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 - 1 L Bottle Label

SCJ Professional
A family company®

NDC 11084-010-66

Refresh™

ANTIBAC FOAM

Citrus Scent Antimicrobial Foam Handwash

Manufactured for: SC Johnson Professional USA, Inc.
Charlotte, NC 28217
1-800-248-7190 www.scjp.com

CITRUS FRAGRANCE

deb
SKIN CARE

1 L
(33.8 fl oz)

Made in Canada
L-1467 R0

PRINCIPAL DISPLAY PANEL - 1 L Bottle Label
REFRESH ANTIBAC FOAM 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-010-400.4 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/12/2017
2NDC:11084-010-271 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/12/2017
3NDC:11084-010-121.2 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/12/2017
4NDC:11084-010-202 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/12/2017
5NDC:11084-010-053.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/12/2017
6NDC:11084-010-010.047 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/27/2019
7NDC:11084-010-55208.2 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product02/27/2019
8NDC:11084-010-960.296 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/01/2019
9NDC:11084-010-661 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/31/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/12/2017
Labeler - SC Johnson Professional USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
APEX International, Inc.015226132manufacture(11084-010)
Establishment
NameAddressID/FEIBusiness Operations
SC Johnson Professional CA Inc.203765300MANUFACTURE(11084-010)

Revised: 12/2022
Document Id: 063ce126-72c2-4dea-b846-b009a7105ba4
Set id: 884d1c8c-5643-423e-8ed4-d2ef38f8af73
Version: 6
Effective Time: 20221209
 
SC Johnson Professional USA, Inc.