BAC-OFF E3

Manufacturer: All American Chemical Company Inc.
Effective date: 2020-06-03
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:16:12

Label at a glance#

ProductBAC-OFF E3

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing. Other information Store between 15-30 0 C (59-86 0 F) Avoid freezing and excessive heat above 40 0 C (104 0 F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

in children less than 2 months of age.
on open skin wounds.

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Store between 15-30⁰C (59-86⁰F)
Avoid freezing and excessive heat above 40⁰C (104⁰F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
582753	ethanol 70 % Topical Solution	PSN	1
582753	ethanol 0.7 ML/ML Topical Solution	SCD	1
582753	ethanol 70 % Topical Solution	SY	1
582753	ethyl alcohol 70 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
28741-001-01	2022-01-28	C162847	48780-1	d6a99b39-73d3-a426-e053-dadaa90af4c2	bc3f705e-4d5c-4b18-bed0-12fea06fed59

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
28741-001-01	BAC-OFF E3	3785 mL in 1 BOTTLE, PLASTIC	SOLUTION	3785		1
28741-001-01	BAC-OFF E3	4 in 1 CASE	SOLUTION	4		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
28741-001	BAC-OFF E3 (ALCOHOL) SOLUTION [ALL AMERICAN CHEMICAL COMPANY INC.]	1	Legacy NDC, 2 package rows	20200605_bc3f705e-4d5c-4b18-bed0-12fea06fed59.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

BAC-OFF E3
Alcohol
GLYCERIN
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
28741-001	28741-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a47fa7d3-9b94-48bd-9ede-d8473893e436			bc3f705e-4d5c-4b18-bed0-12fea06fed59	2020-06-03	Warnings	Exact identifier spl id: a47fa7d3-9b94-48bd-9ede-d8473893e436 spl set id: bc3f705e-4d5c-4b18-bed0-12fea06fed59

Reported adverse events (FAERS/openFDA)#

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