HAND SANITIZER

Manufacturer: Ningbo Venus Cosmetic Co., Ltd.
Effective date: 2020-11-19
Label type: HUMAN OTC DRUG LABEL
Version: 6
Source: full-release
Hydrated at: 2026-05-31 23:33:56

Label at a glance#

ProductHAND SANITIZER

Active ingredientBENZALKONIUM CHLORIDE

Label structure11 sections

Dosage and administration

Spray hand sanitizer in the palm of your hands. Rub briskly product onto hands and allow to dry.

Storage and handling

Store at temperatures below 30°C.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

0.3% Benzalkonium chloride

Purpose

OTC - PURPOSE SECTION

Use when needed.

DIRECTIONS

INDICATIONS & USAGE SECTION

Spray hand sanitizer in the palm of your hands.
Rub briskly product onto hands and allow to dry.

Warnings

WARNINGS SECTION

For external use only. Avoid contact with eyes. If contact occurs, flush eyes with water. If the condition persists, consult a doctor.
If swallowed immediately call a poison control center or a doctor for treatment advice.

Do not use

OTC - DO NOT USE SECTION

OTC - WHEN USING SECTION

For external use only. Avoid contact with eyes. If contact occurs, flush eyes with water. If the condition persists, consult a doctor.

OTC - STOP USE SECTION

If swallowed immediately call a poison control center or a doctor for treatment advice.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray hand sanitizer in the palm of your hands.
Rub briskly product onto hands and allow to dry.

Other information

STORAGE AND HANDLING SECTION

Store at temperatures below 30°C.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerine, Decyl Glucoside, Aloe Vera, Fructooligosaccharide, Fragrance

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

25040050100

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1927027	benzalkonium chloride 0.3 % Topical Spray	PSN	6
1927027	benzalkonium chloride 3 MG/ML Topical Spray	SCD	6
1927027	benzalkonium chloride 0.3 % Topical Spray	SY	6

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
14341-006-01	2022-01-28	C162847	48780-1	d6a99b39-9914-a426-e053-dadaa90af4c2	14341-006 HAND SANITIZER
14341-006-02	2022-01-28	C162847	48780-1	d6a99b39-9914-a426-e053-dadaa90af4c2	14341-006 HAND SANITIZER
14341-006-03	2022-01-28	C162847	48780-1	d6a99b39-9914-a426-e053-dadaa90af4c2	14341-006 HAND SANITIZER
14341-006-04	2022-01-28	C162847	48780-1	d6a99b39-9914-a426-e053-dadaa90af4c2	14341-006 HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
14341-006-01	HAND SANITIZER	50 mL in 1 BOTTLE	SPRAY	50	6
14341-006-02	HAND SANITIZER	100 mL in 1 BOTTLE	SPRAY	100	6
14341-006-03	HAND SANITIZER	250 mL in 1 BOTTLE	SPRAY	250	6
14341-006-04	HAND SANITIZER	400 mL in 1 BOTTLE	SPRAY	400	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
14341-006	HAND SANITIZER SPRAY [NINGBO VENUS COSMETIC CO., LTD.]	6	Legacy NDC, 4 package rows	20201120_a702d5ea-e2d0-ed3b-e053-2a95a90a63fb.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

HAND SANITIZER
GLYCERIN
DECYL GLUCOSIDE
WATER
BENZALKONIUM CHLORIDE
BENZALKONIUM
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
14341-006	14341-006-01, 14341-006-02, 14341-006-03, 14341-006-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
DECYL GLUCOSIDE	Z17H97EA6Y	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
ALOE VERA LEAF	ZY81Z83H0X	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
b47214af-ed46-2dca-e053-2995a90ae000			a702d5ea-e2d0-ed3b-e053-2a95a90a63fb	2020-11-19	Warnings	Exact identifier spl id: b47214af-ed46-2dca-e053-2995a90ae000 spl set id: a702d5ea-e2d0-ed3b-e053-2a95a90a63fb

Reported adverse events (FAERS/openFDA)#

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