Antibacterial Foam

Manufacturer
SC Johnson Professional USA Inc. | APEX International, Inc.
Effective date
2025-12-23
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
full-release
Hydrated at
2026-06-01 01:28:31

Label at a glance#

ProductAntibacterial 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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE, 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

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).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TSFG1-DCN9290 TOTO 1gal Label-v10.jpgTSFG1-DCN9290 TOTO 1gal Label-v10.jpg

TSFG1-DCN9290 TOTO 1gal Label-v10.jpgTSFG1-DCN9290 TOTO 1gal Label-v10.jpg

This product does not contain any prop65 ingredients.

TSFG1

DCN9290

TOTO

Antibacterial Foam Soap

Cleans hands!

Kills germs!

Moisturizes!

Triclosan-free!

One Gallon (3.78 Liters)

Product Features

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

This product contains moisturizers and emollients for the skin making it ideal for frequent use environments.

Manufactured for:

TOTO USA, Inc.

1155 Southern Road

Morrow, GA 30260

888-295-8134

Made in the USA

R00

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN11
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD11
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY11
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY11

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11084-021-05Antibacterial Foam3.78 L in 1 BOTTLE, PLASTICSOLUTION3.7811
11084-021-42Antibacterial Foam18.93 L in 1 PAILSOLUTION18.9311
11084-021-55Antibacterial Foam208.2 L in 1 DRUMSOLUTION208.211

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11084-02111084-021-05, 11084-021-42, 11084-021-55

Ingredients#

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

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

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Antibacterial FoamBENZALKONIUM CHLORIDESC Johnson Professional USA Inc.df36ccda-b9cb-41ba-8d4d-56ec447e63df2025-12-23WarningsExact identifier
ndc (package): 11084-021-55
ndc (package): 11084-021-42
ndc (package): 11084-021-05
ndc (product): 11084-021
ndc11 (package): 11084002155
ndc11 (package): 11084002105
ndc11 (package): 11084002142
spl id: 70390f59-9b71-4614-be06-57ae24e8ec5c
spl set id: df36ccda-b9cb-41ba-8d4d-56ec447e63df

Reported adverse events (FAERS/openFDA)#

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