hand sanitizer

Manufacturer
QUANZHOU BESTHOPE HOUSEHOLD PRODUCTS CO.,LTD.
Effective date
2020-08-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:25:24

Label at a glance#

Producthand sanitizer
Active ingredientALCOHOL
Label structure6 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping Children under 6 years of age use only under adult supervision Not recommended for infants

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Use To reduce bacteria that potentially
Can cause disease.

WARNINGS SECTION

Warnings For external use only. Flammable. Keep away from
heat and flame. Keep out of reach of children. If swallowed, get
medical help or contact a Poison Control Center right away
When using this product
1 Keep out of eyes. In case of contact with eyes, flush thoroughly with water
■Avoid contact with open skin ■ Do not inhale or ingest
Stop use and ask a doctor if skin irritation or redness develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get
medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping
Children under 6 years of age use only under adult supervision
Not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol, Water (Aqua), Glycerin, Butylene Glyool, Carbomer, Aminomethyl
Propanol, Aloe Barbadensis Leaf Extract.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50049-006-01hand sanitizer60 mL in 1 BOTTLEGEL601
50049-006-01hand sanitizer100 in 1 CARTONGEL1001
50049-006-02hand sanitizer100 mL in 1 BOTTLEGEL1001
50049-006-02hand sanitizer60 in 1 CARTONGEL601
50049-006-03hand sanitizer24 in 1 CARTONGEL241
50049-006-03hand sanitizer250 mL in 1 BOTTLEGEL2501
50049-006-04hand sanitizer12 in 1 CARTONGEL121
50049-006-04hand sanitizer500 mL in 1 BOTTLEGEL5001
50049-006-05hand sanitizer998 mL in 1 BOTTLEGEL9981
50049-006-05hand sanitizer6 in 1 CARTONGEL61
50049-006-06hand sanitizer36 in 1 CARTONGEL361
50049-006-06hand sanitizer180 mL in 1 BOTTLEGEL1801
50049-006-07hand sanitizer24 in 1 CARTONGEL241
50049-006-07hand sanitizer200 mL in 1 BOTTLEGEL2001
50049-006-08hand sanitizer300 mL in 1 BOTTLEGEL3001
50049-006-08hand sanitizer24 in 1 CARTONGEL241
50049-006-09hand sanitizer100 in 1 CARTONGEL1001
50049-006-09hand sanitizer50 mL in 1 BOTTLEGEL501
50049-006-10hand sanitizer30 mL in 1 BOTTLEGEL301
50049-006-10hand sanitizer100 in 1 CARTONGEL1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50049-006HAND SANITIZER (ALCOHOL) GEL [QUANZHOU BESTHOPE HOUSEHOLD PRODUCTS CO.,LTD.]1Legacy NDC, 20 package rows20200821_ad584abe-b6a8-4135-e053-2995a90a67d0.zip

Products#

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

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

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
ad584abe-b6a9-4135-e053-2995a90a67d0ad584abe-b6a8-4135-e053-2995a90a67d02020-08-20WarningsExact identifier
spl id: ad584abe-b6a9-4135-e053-2995a90a67d0
spl set id: ad584abe-b6a8-4135-e053-2995a90a67d0

Reported adverse events (FAERS/openFDA)#

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