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 21:05:03

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 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

Do not store above 105°F May discolor some fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease

recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

Flammable

Keep away from fire or flame

OTC - WHEN USING SECTION

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

avoid contact with broken skin

do not inhale or ingest

OTC - STOP USE SECTION

irritation or redness develops

condition persists for more than 72 hours

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

Do not store above 105°F

May discolor some fabrics

Harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, Acrylates Copolymer,Propylene Glycol,Butylene Glycol,Aminomethyl Propanol,Fragrance.

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Package label, principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60mL NDC: 73905-017-01 60mL60mL

500mL NDC: 73905-017-02 500mL500mL

FDA-Initiated Inactive NDC Indexing#

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73905-01773905-017-01, 73905-017-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
165f851c-5c97-d9af-e063-6394a90aedb1a60bdbda-d7bb-17ba-e053-2a95a90a40152024-04-18WarningsExact identifier
spl id: 165f851c-5c97-d9af-e063-6394a90aedb1
spl set id: a60bdbda-d7bb-17ba-e053-2a95a90a4015

Reported adverse events (FAERS/openFDA)#

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