Hand Sanitizer

Manufacturer
NINGBO MEIDI COSMETICS CO., LTD.
Effective date
2020-06-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:08

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Do not store above 105 °F

INACTIVE INGREDIENT SECTION

aqua,glycerin,propylene glycol,carbomer,triethanolamine,red 33,blue 1,yellow 5

INDICATIONS & USAGE SECTION

Wet hands thoroughly with product and rub until dry without wiping.

OTC - ACTIVE INGREDIENT SECTION

ethyl alcohol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

●For external use only.
●Flammable.Keep away from heat and flame.
●Discontinue if skin becomes irritated and ask a doctor.
●Keep out of reach of children.
●In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

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
87269-001-012022-01-28C16284748780-1d6a99b39-7382-a426-e053-dadaa90af4c2a7b6474b-d180-39bb-e053-2a95a90ae247

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87269-001-01Hand Sanitizer500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
87269-001HAND SANITIZER (HAND WASHING) GEL [NINGBO MEIDI COSMETICS CO., LTD.]1Legacy NDC, 1 package rows20200611_a7b6474b-d180-39bb-e053-2a95a90ae247.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87269-00187269-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
a7b6474b-d181-39bb-e053-2a95a90ae247a7b6474b-d180-39bb-e053-2a95a90ae2472020-06-10WarningsExact identifier
spl id: a7b6474b-d181-39bb-e053-2a95a90ae247
spl set id: a7b6474b-d180-39bb-e053-2a95a90ae247

Reported adverse events (FAERS/openFDA)#

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