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Bac Off

Manufacturer
Wayne Concept Manufacturing Co Inc
Effective date
2010-06-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:53:06

Label at a glance#

ProductBac Off
Active ingredientBenzalkonium Chloride
Label structure6 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients                                                          Purpose

Benzalkonium Chloride 0.1%..........................................Antimicrobial

INDICATIONS & USAGE SECTION

Uses:

For hand sanitizing to decrease bacteria on the skin.

Recommended for repeated use.

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

When using this product avoid contact with eyes.

In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

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.

DOSAGE & ADMINISTRATION SECTION

Directions:

Pump a small amount of foam into palms of hand.

Rub thoroughly over all surfaces of both hands.

Rub hands together briskly until dry.

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water (aqua), dihydroxypropyl PEG-5 linoleammonium chloride, glycereth-2-cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Wayne

Select Line

BAC OFF

Instant Foam Hand Sanitizer

Manufactured by:

Wayne Concept Manufacturing Co., Inc.

Fort Wayne, IN 46825        260-482-8615

Net Contents: 1 U.S. Gallon (3.785 L)

Serving the maintenance community since 1933

container labelcontainer label


FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64495-2362-12025-05-14C16284748780-19d75b9cf-d92e-f424-e053-dadaa90a57ceDrug Facts
64495-2362-82025-05-14C16284748780-19d75b9cf-d92e-f424-e053-dadaa90a57ceDrug Facts
64495-2362-12020-01-31C16284748780-19d75b9cf-d92e-f424-e053-dadaa90a57ceDrug Facts
64495-2362-82020-01-31C16284748780-19d75b9cf-d92e-f424-e053-dadaa90a57ceDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Benzalkonium ChlorideACTIVE INGREDIENTF5UM2KM3W71
BenzalkoniumACTIVE MOIETY7N6JUD5X6Y1
Behentrimonium ChlorideINACTIVE INGREDIENTX7GNG3S47T1
Dihydroxyethyl Cocamine OxideINACTIVE INGREDIENT8AR51R3BL51
Dihydroxypropyl Peg-5 Linoleammonium ChlorideINACTIVE INGREDIENT0Y0NQR2GH11
Glycereth-2 CocoateINACTIVE INGREDIENTJWM00VS7HC1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64495-236264495-2362-8, 64495-2362-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
Benzalkonium ChlorideF5UM2KM3W7ACTIB
Water059QF0KO0RIACT
Dihydroxypropyl Peg-5 Linoleammonium Chloride0Y0NQR2GH1IACT
Glycereth-2 CocoateJWM00VS7HCIACT
Behentrimonium ChlorideX7GNG3S47TIACT
Dihydroxyethyl Cocamine Oxide8AR51R3BL5IACT

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
347d8c30-11e3-42a8-e063-6294a90aea0c5fce3a50-3195-4891-a6ac-7b5aef4e80ea2025-05-06WarningsExact identifier
spl set id: 5fce3a50-3195-4891-a6ac-7b5aef4e80ea

Reported adverse events (FAERS/openFDA)#

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