Hand Sanitizer

Manufacturer: BLUE CROSS LABORATORIES
Effective date: 2020-08-06
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:24:00

Label at a glance#

ProductHand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure10 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.12%. Purpose: Antibacterial

Purpose

OTC - PURPOSE SECTION

Antibacterial, Hand Sanitizer

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

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
do not inhale or ingest

Stop use and ask a doctor

OTC - STOP USE SECTION

if skin irritation develops.

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

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, propylene glycol, Aloe barbadensis leaf extract, tocopheryl acetate, fragrance, triethanolamine, carbomer

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

89 mL NDC: 22431-150-01

PDP

236 mL NDC: 22431-150-02

PDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2360876	benzalkonium chloride 0.12 % Topical Gel	PSN	2
2360876	benzalkonium chloride 0.0012 MG/MG Topical Gel	SCD	2
2360876	benzalkonium chloride 0.12 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
22431-150-01	2022-01-28	C162847	48780-1	d6a99b39-445b-a426-e053-dadaa90af4c2	Hand sanitizer
22431-150-02	2022-01-28	C162847	48780-1	d6a99b39-445b-a426-e053-dadaa90af4c2	Hand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
22431-150-01	Hand Sanitizer	89 mL in 1 BOTTLE	GEL	89		2
22431-150-02	Hand Sanitizer	236 mL in 1 BOTTLE	GEL	236		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
22431-150	HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [BLUE CROSS LABORATORIES]	2	Legacy NDC, 2 package rows	20200807_a5339901-0d14-0282-e053-2995a90adc57.zip

Products#

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

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

Hand Sanitizer
Benzalkonium Chloride
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
GLYCERIN
ALPHA-TOCOPHEROL ACETATE
WATER
BENZALKONIUM
TROLAMINE
PROPYLENE GLYCOL
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
22431-150	22431-150-01, 22431-150-02
75729-002

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALPHA-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
TROLAMINE	9O3K93S3TK	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
ALOE VERA LEAF	ZY81Z83H0X	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
ac3cf8a5-b5eb-174f-e053-2995a90a8282			a5339901-0d14-0282-e053-2995a90adc57	2020-08-06	Warnings	Exact identifier spl id: ac3cf8a5-b5eb-174f-e053-2995a90a8282 spl set id: a5339901-0d14-0282-e053-2995a90adc57

Reported adverse events (FAERS/openFDA)#

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