Alcohol Free Hand Sanitizer

Manufacturer: HAIAN KANGRUI TEXTILE CO., LTD.
Effective date: 2025-08-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:10:05

Label at a glance#

ProductAlcohol Free Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Indications and uses

For hand sanitizing to reduce bacteria on the skin.

Dosage and administration

Squeeze small amount in your palm and briskly rub hands together until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.3%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire and flame.

When using this product，

OTC - WHEN USING SECTION

do not use in or near the eyes.In case of contact，rinse eyes thoroughly with water.

Discontinue use

OTC - STOP USE SECTION

if irritation or redness 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

Squeeze small amount in your palm and briskly rub hands together until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, POLYOXYL 40 HYDROGENATED CASTOR OIL, HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%), GLYCERIN, PHENOXYETHANOL, FRAGRANCE.

87001-004-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

87001-004-01

87001-004-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

87001-004-02

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2368187	benzalkonium chloride 0.3 % Topical Gel	PSN	1
2368187	benzalkonium chloride 0.003 MG/MG Topical Gel	SCD	1
2368187	benzalkonium chloride 0.3 % Topical Gel	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
87001-004-01	Alcohol Free Hand Sanitizer	15 mL in 1 BOTTLE	GEL	15		1
87001-004-02	Alcohol Free Hand Sanitizer	30 mL in 1 BOTTLE	GEL	30		1

Products#

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

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

Alcohol Free Hand Sanitizer
BENZALKONIUM CHLORIDE
WATER
BENZALKONIUM
HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%)
GLYCERIN
PHENOXYETHANOL
POLYOXYL 40 HYDROGENATED CASTOR OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
87001-004	87001-004-01, 87001-004-02

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%)	X70SE62ZAR	IACT
GLYCERIN	PDC6A3C0OX	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
POLYOXYL 40 HYDROGENATED CASTOR OIL	7YC686GQ8F	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
Alcohol Free Hand Sanitizer	BENZALKONIUM CHLORIDE	HAIAN KANGRUI TEXTILE CO., LTD.	3c273544-4562-8f37-e063-6394a90ab4d3	2025-08-12	Warnings	Exact identifier ndc (package): 87001-004-02 ndc (package): 87001-004-01 ndc (product): 87001-004 ndc11 (package): 87001000401 ndc11 (package): 87001000402 spl id: 3c27353a-d762-8c1f-e063-6394a90ae38e spl set id: 3c273544-4562-8f37-e063-6394a90ab4d3

Reported adverse events (FAERS/openFDA)#

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