FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Jinhua City Wellmae Cosmetics Co., Ltd.
Effective date
2022-01-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:47:13

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Wet hands thoroughly and rub together until dry. Not recommended for infants

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Alcohol 62% Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

Stop using this product and ask a doctor if: irritation or redness develops and lasts.

OTC - WHEN USING SECTION

When using this product:Avoid contact with eyes. If contact occurs, rinse with water.

OTC - STOP USE SECTION

Stop using this product and ask a doctor if: irritation or redness develops and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, cet med al help or contact a Poison Control Center immediatelly

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly and rub together until dry. Not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA,Propylene Glycol,Carbopol 940

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN3
1305100ethanol 0.75 ML/ML Topical GelSCD3
1305100ethanol 75 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75427-002-012024-01-30C16284748780-10191ceaa-6cdc-198a-e063-dbdaa90aec3e75427-002 Hand Sanitizer
75427-002-022024-01-30C16284748780-10191ceaa-6cdc-198a-e063-dbdaa90aec3e75427-002 Hand Sanitizer
75427-002-012023-11-09C16284748780-10191ceaa-6cdc-198a-e063-dbdaa90aec3e75427-002 Hand Sanitizer
75427-002-022023-11-09C16284748780-10191ceaa-6cdc-198a-e063-dbdaa90aec3e75427-002 Hand Sanitizer
75427-002-012023-07-28C16284748780-10191ceaa-6cdc-198a-e063-dbdaa90aec3e75427-002 Hand Sanitizer
75427-002-022023-07-28C16284748780-10191ceaa-6cdc-198a-e063-dbdaa90aec3e75427-002 Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75427-002-01Hand Sanitizer29 mL in 1 BOTTLEGEL293
75427-002-02Hand Sanitizer50 mL in 1 BOTTLEGEL503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75427-002HAND SANITIZER (ALCOHOL) GEL [JINHUA CITY WELLMAE COSMETICS CO., LTD.]3Legacy NDC, 2 package rows20220120_a3decd34-5e09-1033-e053-2a95a90a9640.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75427-00275427-002-01, 75427-002-02

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
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER COPOLYMER TYPE A71DD5V995LIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML · Source PDF

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
d5fb82fb-7fa4-764f-e053-2a95a90a0656a3decd34-5e09-1033-e053-2a95a90a96402022-01-19WarningsExact identifier
spl id: d5fb82fb-7fa4-764f-e053-2a95a90a0656
spl set id: a3decd34-5e09-1033-e053-2a95a90a9640

Reported adverse events (FAERS/openFDA)#

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