Breathe Hand Sanitizer Gel

Manufacturer: Blue Cross Laboratories, Inc.
Effective date: 2020-10-06
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:31:11

Label at a glance#

ProductBreathe Hand Sanitizer Gel

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping. for children under 6 use only under supervision not recommended for infants

Storage and handling

do not store above 105 F may discolor some fabrics harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease.
recommended for repeated use

Warnings

WARNINGS SECTION

For external use only- hands

Flammable. Keep away from heat or flame

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water.

avoid contact with broken skin. do not inhale or ingest.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation 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

wet hands thoroughly with product and allow to dry without wiping.
for children under 6 use only under supervision
not recommended for infants

Other information

STORAGE AND HANDLING SECTION

do not store above 105 F
may discolor some fabrics
harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, fragrance, carbopol, triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

breathe Hand Sanitizer Gel

8 FL OZ (236 mL)

Breathe Hand Santizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
22431-010-01	2022-01-28	C162847	48780-1	d6a99b39-c994-a426-e053-dadaa90af4c2	Breathe Hand Sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
22431-010-01	Breathe Hand Sanitizer Gel	236 mL in 1 BOTTLE	GEL	236		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
22431-010	BREATHE HAND SANITIZER GEL (ALCOHOL) GEL [BLUE CROSS LABORATORIES, INC.]	1	Legacy NDC, 1 package rows	20201008_b102f8d7-a9c9-393e-e053-2a95a90a9cd0.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Breathe Hand Sanitizer Gel
ALCOHOL
GLYCERIN
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
WATER
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
22431-010	22431-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
TROLAMINE	9O3K93S3TK	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
b102fc86-1640-3595-e053-2a95a90a332b			b102f8d7-a9c9-393e-e053-2a95a90a9cd0	2020-10-06	Warnings	Exact identifier spl id: b102fc86-1640-3595-e053-2a95a90a332b spl set id: b102f8d7-a9c9-393e-e053-2a95a90a9cd0

Reported adverse events (FAERS/openFDA)#

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