FDA.reportPublic FDA data

Antibacterial Foam

Manufacturer
SC Johnson Professional USA, Inc.
Effective date
2020-11-25
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:05:34

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.

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

58252-Chemstar AeroGreen-NewFormula-V8.jpg58252-Chemstar AeroGreen-NewFormula-V8.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)

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
11084-01311084-013-27

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
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
LACTIC ACID33X04XA5ATIACT
SALICYLIC ACIDO414PZ4LPZIACT
D&C GREEN NO. 58J6RDU8L9XIACT
FD&C YELLOW NO. 5I753WB2F1MIACT

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
3882491e-e88d-47de-9544-79e5f643402f67d75cc7-24b3-428a-9e6b-9b62c393776a2020-11-25WarningsExact identifier
spl id: 3882491e-e88d-47de-9544-79e5f643402f
spl set id: 67d75cc7-24b3-428a-9e6b-9b62c393776a

Reported adverse events (FAERS/openFDA)#

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