Alcohol Free Hand Sanitizer

Manufacturer: Zhejiang Ayan Biotech Co.,Ltd.
Effective date: 2023-11-06
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 21:21:36

Label at a glance#

ProductAlcohol Free Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Indications and uses

For hand washing to decrease bacteria on the skin.

Dosage and administration

Wet hands thoroughly with a product and allow to dry without wiping.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, rinse with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

skin irritation and redness develops and persists.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help promptly and contact Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with a product and allow to dry without wiping.

Other Information

SPL UNCLASSIFIED SECTION

Store under 105 F. ^o

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Polyquaternium-10, Propylene Glycol, Glycerin, Polyaminopropyl Biguanide, PEG-40 Hydrogenated Castor Oil, Fragrance, Tromethamine

Package Labeling: 70412-150-10

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70412-150-10

Package Labeling: 70412-150-20

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70412-150-20

Products#

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

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

Alcohol Free Hand Sanitizer
BENZALKONIUM CHLORIDE
WATER
PROPYLENE GLYCOL
GLYCERIN
POLYAMINOPROPYL BIGUANIDE
POLYOXYL 40 HYDROGENATED CASTOR OIL
TROLAMINE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70412-150	70412-150-10, 70412-150-20

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
WATER	059QF0KO0R	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
GLYCERIN	PDC6A3C0OX	IACT
POLYAMINOPROPYL BIGUANIDE	DT9D8Z79ET	IACT
POLYOXYL 40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT
TROLAMINE	9O3K93S3TK	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

Source Document#

Source XML · Source PDF

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
125e7ee9-aeec-9df9-e063-6394a90a6b5e			7bdc4487-31c4-47c8-9d18-151cecdb11f4	2024-02-27	Warnings	Exact identifier spl set id: 7bdc4487-31c4-47c8-9d18-151cecdb11f4

Reported adverse events (FAERS/openFDA)#

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