Alcohol Free Hand Sanitizer

Manufacturer: NANTONG QINJI HEALTH TECHNOLOGY CO., LTD | NANTONG QINJI HEALTH TECHNOLOGY CO., LTD.
Effective date: 2024-08-19
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 20:56:26

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 ingredients

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.

Warinings

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, Glycerin, Cellulose, Triethanolamine, Ethoxylated hydrogenated castor oil, Fragrance.

84641-004-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

84641-004-01

84641-004-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

84641-004-02

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

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84641-004	84641-004-01, 84641-004-02

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
HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%)	X70SE62ZAR	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
POLYOXYL 40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT
PHENOXYETHANOL	HIE492ZZ3T	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
20140907-a457-4d46-e063-6294a90af018			1fa05d6c-0ad7-9986-e063-6294a90aeb26	2024-08-19	Warnings	Exact identifier spl id: 20140907-a457-4d46-e063-6294a90af018 spl set id: 1fa05d6c-0ad7-9986-e063-6294a90aeb26

Reported adverse events (FAERS/openFDA)#

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