Hand Sanitizer

Manufacturer
Zhejiang Meimi Technology Co., Ltd.
Effective date
2020-04-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:50

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Keep away from flame or high heat.

INACTIVE INGREDIENT SECTION

Water(Aqua, Eau.)

Propylene Glycol

Carbomer

Fragrance (Parfum)

Tocopheryl Acetate

DISODIUM EDTA

Linalool

INDICATIONS & USAGE SECTION

Put enough product in your palm to cover hands and rub hands together briskly until dry Children should be supervised when using Hand Sanitizer.

OTC - ACTIVE INGREDIENT SECTION

alcohol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of children

OTC - PURPOSE SECTION

Disinfection
Sterilization

WARNINGS SECTION

Keep away from flame or high heat.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41366-001-012022-01-28C16284748780-1d6a99b39-7036-a426-e053-dadaa90af4c2a38949bb-c212-474a-e053-2a95a90ad1ce

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41366-001-01Hand Sanitizer60 mL in 1 BOTTLEGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41366-001HAND SANITIZER GEL [ZHEJIANG MEIMI TECHNOLOGY CO., LTD.]1Legacy NDC, 1 package rows20200418_a38949bb-c212-474a-e053-2a95a90ad1ce.zip

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
41366-00141366-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
a38949bb-c213-474a-e053-2a95a90ad1cea38949bb-c212-474a-e053-2a95a90ad1ce2020-04-15WarningsExact identifier
spl id: a38949bb-c213-474a-e053-2a95a90ad1ce
spl set id: a38949bb-c212-474a-e053-2a95a90ad1ce

Reported adverse events (FAERS/openFDA)#

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