62% alcohol hand sanitizer

Manufacturer
Ultra Distributors Inc | Ultra Distributors | Ningbo Home Solution Corp., LTD
Effective date
2021-12-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:45:54

Label at a glance#

Product62% alcohol hand sanitizer
Active ingredientALCOHOL
Label structure7 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

OTC - ACTIVE INGREDIENT SECTION

Alcohol62%

INDICATIONS & USAGE SECTION

Directions: Pour a sufficient amount of the liquid into the palm of your dry hands. Rub thoroughly all over hands briskly until dry. Repeat if necessary. Use without water. Use only under adult supervision.

WARNINGS SECTION

Warnings: Highly flammable liquid and vapour. Causes serious eye iritation. May cause skin iritation. Keep away from heat, sparks, hot surfaces, fire, open flame and sources of ignition. No smoking. Keep at room temperature. Store in a well-ventilated, cool and dry place, away from direct sunlight. Do not store above 40 °C

For external use only.

Avoid contact with eyes. If in eyes, rinse immediately with clean water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Do not swallow. If swallowed, rinse mouth and seek medical advice immediately and show this label. Do not induce vomiting. Do not use on damage, inflamed or broken skin. If iritation or redness develops, discontinue use.

Keep out of the reach of babies, children & animals.

DOSAGE & ADMINISTRATION SECTION

236ml store in ventilated shade and Do not store above 40 °C

INACTIVE INGREDIENT SECTION

Alcohol, water/eau/aqua, carbomer,triethanolamine, propylene glycol, glycerin

Front Panel and Back Panel Art

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78495-015-0162% alcohol hand sanitizer236 mL in 1 BOTTLEGEL2362

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78495-01562% ALCOHOL HAND SANITIZER (HAND SANITIZER) GEL [ULTRA DISTRIBUTORS INC]2Legacy NDC, 1 package rows20211224_a838bab3-67be-213f-e053-2a95a90ab2d5.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78495-01578495-015-01

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
d3d7b17e-d243-7ccb-e053-2a95a90addfda838bab3-67be-213f-e053-2a95a90ab2d52021-12-23WarningsExact identifier
spl id: d3d7b17e-d243-7ccb-e053-2a95a90addfd
spl set id: a838bab3-67be-213f-e053-2a95a90ab2d5

Reported adverse events (FAERS/openFDA)#

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