FDA.reportPublic FDA data

Antibac-4000

Manufacturer
Kramer Detergents
Effective date
2022-01-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:12:03

Label at a glance#

ProductAntibac-4000
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Dosage and administration

• Use with foaming pump or dispenser • Lather for at least 15 seconds, then rinse

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product: Avoid contact with eyes. In case of eye contact, flush with water

PATIENT COUNSELING INFORMATION

Stop use and ask a doctor if irritation or redness develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

• Use with foaming pump or dispenser

• Lather for at least 15 seconds, then rinse

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Cocamidopropyl Betaine, Citric Acid, Alpha Olefin Sulfonate, Sodium Lauryl Ether Sulfate, Sodium Chloride.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANTIBAC-4000 item #7009

HAND SOAP

USE WITH COUNTER OR WALL DISPENSER

KILLS 99.99% OF MOST COMMON GERMS

REGULAR • FRESH SCENT • GENTLE

Distributed by Kramer Detergents Fayetteville AR 72701 / 888-280-7075

NDC 66868-103-01 | FDA Registered NET CONTENTS: 1 GALLON (3.87 L)

1 gallon label1 gallon label

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
66868-10366868-103-01, 66868-103-05, 66868-103-15, 66868-103-65, 66868-103-55

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
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)S38J6RZN16IACT
LAURAMINE OXIDE4F6FC4MI8WIACT
COCO DIISOPROPANOLAMIDES485AM948QIACT
FD&C RED NO. 40WZB9127XOAIACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
WATER059QF0KO0RIACT

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
ee6bb0b9-2053-7ba0-e053-2995a90a3cd2a80ef4dd-315d-168b-e053-2a95a90ab31a2022-11-26WarningsExact identifier
spl set id: a80ef4dd-315d-168b-e053-2a95a90ab31a

Reported adverse events (FAERS/openFDA)#

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