FDA.reportPublic FDA data

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

Wash hands to remove soil dispense palmful spread to cover hands, rub in well air dry, do not rinse or towel dry

Storage and handling

for additional information, see Safety Data Sheet (SDS) EMERGENCY HEALTH INFORMATION: 1 800 328 0026. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US).

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Antiseptic handwash

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Flammable

Keep away from fire or flame, heat, sparks, and sources of static discharge.

When using this product

OTC - WHEN USING SECTION

If in eyes, rinse promptly and thoroughly with water

discontinue use if irritation and redness develop

Do not use

OTC - DO NOT USE SECTION

in eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

eye or skin irritation or redness occurs 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

Wash hands to remove soil

dispense palmful

spread to cover hands, rub in well

air dry, do not rinse or towel dry

Other information

STORAGE AND HANDLING SECTION

for additional information, see Safety Data Sheet (SDS)

EMERGENCY HEALTH INFORMATION: 1 800 328 0026. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US).

Inactive ingredients

INACTIVE INGREDIENT SECTION

water (aqua), propylene glycol, glycerin, acrylates/C10-30 alkyl acrylate crosspolymer, aminomethyl propanol, denatonium benzoate

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v (equivalent to 62.5% w/w)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500mL NDC: 73905-024-01 500mL500mL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73905-024-012024-04-18C16284748780-1d6a99b39-9121-a426-e053-dadaa90af4c2ab78e302-aa6a-fdb0-e053-2995a90ae564
73905-024-022024-04-18C16284748780-1d6a99b39-9121-a426-e053-dadaa90af4c2ab78e302-aa6a-fdb0-e053-2995a90ae564
73905-024-012024-01-30C16284748780-1d6a99b39-9121-a426-e053-dadaa90af4c2ab78e302-aa6a-fdb0-e053-2995a90ae564
73905-024-022024-01-30C16284748780-1d6a99b39-9121-a426-e053-dadaa90af4c2ab78e302-aa6a-fdb0-e053-2995a90ae564
73905-024-012022-03-06C16284748780-1d6a99b39-9121-a426-e053-dadaa90af4c2ab78e302-aa6a-fdb0-e053-2995a90ae564
73905-024-022022-03-06C16284748780-1d6a99b39-9121-a426-e053-dadaa90af4c2ab78e302-aa6a-fdb0-e053-2995a90ae564
73905-024-012022-01-28C16284748780-1d6a99b39-9121-a426-e053-dadaa90af4c2ab78e302-aa6a-fdb0-e053-2995a90ae564
73905-024-022022-01-28C16284748780-1d6a99b39-9121-a426-e053-dadaa90af4c2ab78e302-aa6a-fdb0-e053-2995a90ae564

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
73905-02473905-024-01, 73905-024-02

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
NameUNIIKind
WATER059QF0KO0RIACT
(C10-C30)ALKYL METHACRYLATE ESTERXH2FQZ38D8IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB
DENATONIUM BENZOATE4YK5Z54AT2IACT

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
165f739a-99df-9a19-e063-6294a90af323ab78e302-aa6a-fdb0-e053-2995a90ae5642024-04-18WarningsExact identifier
spl id: 165f739a-99df-9a19-e063-6294a90af323
spl set id: ab78e302-aa6a-fdb0-e053-2995a90ae564

Reported adverse events (FAERS/openFDA)#

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