Hand sanitizer

Manufacturer: Welch Materials (Zhejiang), Inc.
Effective date: 2020-12-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:35:42

Label at a glance#

ProductHand sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure6 sections

Dosage and administration

Take an appropriate amount of disinfectant to the palm, rub according to the hand disinfection code instructions, ensure that the sanitizer completely covers the skin of the hand sand wait for one minute until dry

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.3%

Purpose

OTC - PURPOSE SECTION

Antibacterial

USE

INDICATIONS & USAGE SECTION

Suitable for sanitary hand disinfection.

Warning

WARNINGS SECTION

When using this product, avoid entering into the eyes.

Do not rub the eyes if accidental contact, rinse the eyes thoroughly with water for 15 minutes.

Those with silver allergies shall use with caution.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, seek medical help or contact a Poison Control Center immediately.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, Glycerol, Silver Ion

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 ml NDC 81242-001-01 50100ml NDC 81242-001-02 100

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81242-001-01	2023-01-30	C162847	48780-1	f386c64a-3f1e-0266-e053-dadaa90a7c1a	yuexu 0.13% BENZALKONIUM CHLORIDE
81242-001-02	2023-01-30	C162847	48780-1	f386c64a-3f1e-0266-e053-dadaa90a7c1a	yuexu 0.13% BENZALKONIUM CHLORIDE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81242-001-01	Hand sanitizer	50 mL in 1 BOTTLE	SPRAY	50		1
81242-001-02	Hand sanitizer	100 mL in 1 BOTTLE	SPRAY	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81242-001	HAND SANITIZER (BENZALKONIUM CHLORIDE) SPRAY [WELCH MATERIALS (ZHEJIANG), INC.]	1	Legacy NDC, 2 package rows	20201223_b6f595fc-bb2a-b5e0-e053-2a95a90a3a83.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Hand sanitizer
BENZALKONIUM CHLORIDE
WATER
SILVER CHLORIDE
GLYCERIN
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81242-001	81242-001-01, 81242-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SILVER CHLORIDE	MWB0804EO7	IACT
GLYCERIN	PDC6A3C0OX	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
b6f595fc-bb2b-b5e0-e053-2a95a90a3a83			b6f595fc-bb2a-b5e0-e053-2a95a90a3a83	2020-12-21	Warnings	Exact identifier spl id: b6f595fc-bb2b-b5e0-e053-2a95a90a3a83 spl set id: b6f595fc-bb2a-b5e0-e053-2a95a90a3a83

Reported adverse events (FAERS/openFDA)#

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