Hand Sanitizer

Manufacturer
Dongguan City Dexu Toys Co.,Ltd
Effective date
2020-05-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:13:51

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

for handwashing to decrease bacteria on the skin

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping

Storage and handling

Store under 105℉

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% Purpose: Antibactirial

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

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

OTC - DO NOT USE SECTION

do not use in eyes.In case of contact with eye rinse with water

OTC - WHEN USING SECTION

when using this product do not use in eyes.In case of contact with eye rinse with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develop and persist

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help promiptly

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping

Other information

STORAGE AND HANDLING SECTION

Store under 105℉

Inactive ingredients

INACTIVE INGREDIENT SECTION

ALOE BARBADENSIS LEAF,carbomer,dimethicone,triisopropanolamine,water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50mL NDC: 78048-001-01 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
78048-001-012022-01-28C16284748780-1d6a99b39-f2ee-a426-e053-dadaa90af4c2hand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78048-001-01Hand Sanitizer50 mL in 1 BOTTLEGEL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78048-001HAND SANITIZER (ALCOHOL) GEL [DONGGUAN CITY DEXU TOYS CO.,LTD]1Legacy NDC, 1 package rows20200520_a60d0b61-d166-0fad-e053-2a95a90a6707.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
78048-00178048-001-01

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
a60cf263-6b3b-4f85-e053-2995a90a2b9fa60d0b61-d166-0fad-e053-2a95a90a67072020-05-19WarningsExact identifier
spl id: a60cf263-6b3b-4f85-e053-2995a90a2b9f
spl set id: a60d0b61-d166-0fad-e053-2a95a90a6707

Reported adverse events (FAERS/openFDA)#

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