AgroBac Pure FOAM

Manufacturer
SC Johnson Professional USA, Inc. | APEX International, Inc.
Effective date
2024-12-20
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:48:28

Label at a glance#

ProductAgroBac Pure FOAM
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

for hand washing to reduce bacteria on the skin

Dosage and administration

apply to dry hands add water lather hands for 30 seconds rinse and 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 hand washing to reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

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 to dry hands

add water

lather hands for 30 seconds

rinse and dry hands thoroughly

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Hexylene Glycol, Coco-Glucoside, Cocamidopropyl PG-Dimonium Chloride Phosphate, Laurtrimonium Chloride, PEG-6 Cocamide, Citric Acid

PRINCIPAL DISPLAY PANEL - 1 L Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SCJ PROFESSIONAL
A Family Company™

NDC 11084-024-27

AgroBac™ PURE

ANTIMICROBIAL FOAM SOAP
Dye & Fragrance-Free E2 Antibacterial Foam Handwash.

NSF®
Nonfood Compounds
Program Listed E2
157532

1 L (33.8 fl oz)

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

Pat.www.scjp.com/patents

deb
SKIN CARE

1000002834/0320

PRINCIPAL DISPLAY PANEL - 1 L Bottle Label
PRINCIPAL DISPLAY PANEL - 1 L Bottle Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11084-024-01AgroBac Pure FOAM47 mL in 1 BOTTLE, PLASTICSOLUTION475
11084-024-12AgroBac Pure FOAM1200 mL in 1 BOTTLE, PLASTICSOLUTION12005
11084-024-20AgroBac Pure FOAM2000 mL in 1 BOTTLE, PLASTICSOLUTION20005
11084-024-27AgroBac Pure FOAM1000 mL in 1 BOTTLE, PLASTICSOLUTION10005
11084-024-66AgroBac Pure FOAM1000 mL in 1 BOTTLESOLUTION10005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11084-024AGROBAC PURE FOAM (BENZALKONIUM CHLORIDE) SOLUTION [SC JOHNSON PROFESSIONAL USA, INC.]5Current NDC, Legacy NDC, 5 package rows20241225_8b70a920-e63a-418f-8b79-f57eb5576b1a.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11084-02411084-024-27, 11084-024-20, 11084-024-12, 11084-024-01, 11084-024-66

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
AgroBac Pure FOAMBENZALKONIUM CHLORIDESC Johnson Professional USA, Inc.8b70a920-e63a-418f-8b79-f57eb5576b1a2024-12-20WarningsExact identifier
ndc (package): 11084-024-27
ndc (package): 11084-024-20
ndc (package): 11084-024-66
ndc (package): 11084-024-01
ndc (package): 11084-024-12
ndc (product): 11084-024
ndc11 (package): 11084002401
ndc11 (package): 11084002420
ndc11 (package): 11084002412
ndc11 (package): 11084002427
ndc11 (package): 11084002466
spl id: ead64127-9612-4ee5-9059-ab728322ea84
spl set id: 8b70a920-e63a-418f-8b79-f57eb5576b1a

Reported adverse events (FAERS/openFDA)#

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