Guard Alcohol-Free Hand Sanitizer

Manufacturer: Apollo Health and Beauty Care Inc.
Effective date: 2020-04-20
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:07:01

Label at a glance#

ProductGuard Alcohol-Free Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Indications and uses

to help reduce bacteria on the skin. For use when soap and water are not available.

Dosage and administration

put enough product in your palm to cover hands, rub hands together for at least 30 seconds. Allow to dry. Children under 6 years should be supervised when using this product.

Contacts and useful links#

PhoneLabel contact1-866-695-3030

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to help reduce bacteria on the skin. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Do not use

OTC - DO NOT USE SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation develops

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, call or contact a Poison Control Center or get medical help right away.

Directions

DOSAGE & ADMINISTRATION SECTION

put enough product in your palm to cover hands, rub hands together for at least 30 seconds. Allow to dry.
Children under 6 years should be supervised when using this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Hydroxyethylcellulose, Tetrasodium EDTA, Citric Acid, Sodium Hydroxide, DMDM Hydantoin.

Questions?

OTC - QUESTIONS SECTION

1-866-695-3030

Label copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of the label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1098199	benzalkonium chloride 0.13 % Topical Gel	PSN	1
1098199	benzalkonium chloride 0.0013 MG/MG Topical Gel	SCD	1
1098199	benzalkonium chloride 0.13 % Topical Gel	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63148-514-02	2024-01-30	C162847	48780-1	1030e365-1864-111a-e063-dadaa90a10e2	Drug Facts
63148-514-08	2024-01-30	C162847	48780-1	1030e365-1864-111a-e063-dadaa90a10e2	Drug Facts
63148-514-32	2024-01-30	C162847	48780-1	1030e365-1864-111a-e063-dadaa90a10e2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
63148-514-02	Guard Alcohol-Free Hand Sanitizer	59 mL in 1 BOTTLE, PLASTIC	GEL	59	1
63148-514-08	Guard Alcohol-Free Hand Sanitizer	236 mL in 1 BOTTLE, PLASTIC	GEL	236	1
63148-514-32	Guard Alcohol-Free Hand Sanitizer	946 mL in 1 BOTTLE, PLASTIC	GEL	946	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63148-514	GUARD ALCOHOL-FREE HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [APOLLO HEALTH AND BEAUTY CARE INC.]	1	Legacy NDC, 3 package rows	20200421_00b1c798-f5af-4536-8dc4-c60b8b2c0708.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Guard Alcohol-Free Hand Sanitizer
Benzalkonium chloride
BENZALKONIUM
WATER
HYDROXYETHYL CELLULOSE (5000 CPS AT 1%)
EDETATE SODIUM
CITRIC ACID MONOHYDRATE
SODIUM HYDROXIDE
DMDM HYDANTOIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63148-514	63148-514-02, 63148-514-08, 63148-514-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
HYDROXYETHYL CELLULOSE (5000 CPS AT 1%)	X70SE62ZAR	IACT
EDETATE SODIUM	MP1J8420LU	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
DMDM HYDANTOIN	BYR0546TOW	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
9e7da0d1-fd83-42dc-b5c8-b16f0d8c0e9b			00b1c798-f5af-4536-8dc4-c60b8b2c0708	2020-04-20	Warnings	Exact identifier spl id: 9e7da0d1-fd83-42dc-b5c8-b16f0d8c0e9b spl set id: 00b1c798-f5af-4536-8dc4-c60b8b2c0708

Reported adverse events (FAERS/openFDA)#

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