Hand Sanitizer

Manufacturer
ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD
Effective date
2024-04-18
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:05:05

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all surfaces.Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 59-86°F(15-30°C) Avoid freezing and excessive heat above 104°F(40°C)

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Ethyl alcohol 70% v/v. Purpose: Antiseptic

Use

INDICATIONS & USAGE SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing.

Warnings

WARNINGS SECTION

For external use only

Flammable

Keep away from fire or flame

OTC - WHEN USING SECTION

Keep out of eyes, ears and mouth.

In case of contact with eyes,flush thoroughly with water.

OTC - DO NOT USE SECTION

In children less than 2 months of age

on open skin wounds

OTC - STOP USE SECTION

irritation or rash occurs.

This may be signs of a serious condition.

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

Place enough product on hands to cover all surfaces.Rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

Store between 59-86°F(15-30°C)

Avoid freezing and excessive heat above 104°F(40°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water,Propylene glycol, glycerin, carbomer, triethanolamine.

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v. Purpose: Antiseptic

Package label, principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

980mL NDC: 73905-018-01 980mL980mL

500mL NDC: 73905-018-02 500mL500mL236mL NDC: 73905-018-03 236mL236mL

FDA-Initiated Inactive NDC Indexing#

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73905-01873905-018-01, 73905-018-02, 73905-018-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
165f6c0f-f30f-7904-e063-6294a90ac99bab78faea-c844-33ed-e053-2995a90ac1262024-04-18WarningsExact identifier
spl id: 165f6c0f-f30f-7904-e063-6294a90ac99b
spl set id: ab78faea-c844-33ed-e053-2995a90ac126

Reported adverse events (FAERS/openFDA)#

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