Drug Facts

Manufacturer: SC Johnson Professional USA Inc. | APEX International, Inc. | SC Johnson Professional CA Inc.
Effective date: 2026-08-13
Label type: HUMAN OTC DRUG LABEL
Version: 12
Source: daily-update
Hydrated at: 2026-08-18 02:02:58

Label at a glance#

ProductRefresh AntiBac FOAM

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Indications and uses

for handwashing to reduce bacteria on the skin

Dosage and administration

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

Contacts and useful links#

PhoneLabel contact1-800-248-7190

Websitewww.scjp.com

www.scjp.com

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE, 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

for handwashing to reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

INSTRUCTIONS FOR USE SECTION

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of eye contact, flush with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0069124050070	GTIN-13: 0069124050070 EAN-13: 0069124050070 GTIN-12: 069124050070 UPC-A: 069124050070 GTIN storage (14 digits): 00069124050070	refresh-01.jpg

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

Refresh AntiBac FOAM
Benzalkonium Chloride
BENZALKONIUM
WATER
GLYCERIN
LAURAMINE OXIDE
BUTYLENE GLYCOL
LACTIC ACID, UNSPECIFIED FORM
SALICYLIC ACID
D&C GREEN NO. 5
FD&C YELLOW NO. 5

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11084-010	11084-010-40, 11084-010-27, 11084-010-12, 11084-010-20, 11084-010-05, 11084-010-01, 11084-010-55, 11084-010-96, 11084-010-66

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
LAURAMINE OXIDE	4F6FC4MI8W	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
LACTIC ACID, UNSPECIFIED FORM	33X04XA5AT	IACT
SALICYLIC ACID	O414PZ4LPZ	IACT
D&C GREEN NO. 5	8J6RDU8L9X	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
10	2025-12-23	full-release	2026-06-01 01:28:26

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Refresh AntiBac FOAM	BENZALKONIUM CHLORIDE	SC Johnson Professional USA Inc.	884d1c8c-5643-423e-8ed4-d2ef38f8af73	2026-08-13	Warnings	Exact identifier ndc (package): 11084-010-05 ndc (package): 11084-010-01 ndc (package): 11084-010-40 ndc (package): 11084-010-66 ndc (package): 11084-010-96 ndc (package): 11084-010-12 ndc (package): 11084-010-55 ndc (package): 11084-010-20 ndc (package): 11084-010-27 ndc (product): 11084-010 ndc11 (package): 11084001040 ndc11 (package): 11084001005 ndc11 (package): 11084001066 ndc11 (package): 11084001055 ndc11 (package): 11084001001 ndc11 (package): 11084001027 ndc11 (package): 11084001096 ndc11 (package): 11084001020 ndc11 (package): 11084001012 spl id: 1efa3243-2522-4796-9891-a61fc315ea00 spl set id: 884d1c8c-5643-423e-8ed4-d2ef38f8af73

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.