HAND SANITIZER

Manufacturer
Jinhua City Wellmae Cosmetics Co., Ltd.
Effective date
2022-01-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:47:15

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

●Hand sanitizer to help reduce bacteria. ●For use when soap and water are not available

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℃) Do not store above 104°F (40℃)

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

●Hand sanitizer to help reduce bacteria.
●For use when soap and water are not available

WARNINGS

WARNINGS SECTION

For External Use Only. Flammable. Keep Away From Heat Or Flame.

Do not use

OTC - DO NOT USE SECTION

●on children less than 2 months of age.
●on open skin wounds.

When using this product

OTC - WHEN USING SECTION

keep out of ears, eyes and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children

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℃)

Do not store above 104°F (40℃)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Carbopol 940, Glycerine, Propylene GlycoL, Triethanolamine, Water (Aqua)

Package Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ininoutout

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75427-013-012024-01-30C16284748780-10191ceaa-65a2-198a-e063-dbdaa90aec3e75427-013 HAND SANITIZER
75427-013-012023-11-09C16284748780-10191ceaa-65a2-198a-e063-dbdaa90aec3e75427-013 HAND SANITIZER
75427-013-012023-07-28C16284748780-10191ceaa-65a2-198a-e063-dbdaa90aec3e75427-013 HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75427-013-01HAND SANITIZER59 mL in 1 BOTTLEGEL592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75427-013HAND SANITIZER GEL [JINHUA CITY WELLMAE COSMETICS CO., LTD.]2Legacy NDC, 1 package rows20220120_ab7eeed2-8549-0f92-e053-2a95a90ad3cc.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75427-01375427-013-01

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
d5fde120-b2b5-12b8-e053-2995a90ab714ab7eeed2-8549-0f92-e053-2a95a90ad3cc2022-01-20WarningsExact identifier
spl id: d5fde120-b2b5-12b8-e053-2995a90ab714
spl set id: ab7eeed2-8549-0f92-e053-2a95a90ad3cc

Reported adverse events (FAERS/openFDA)#

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