hand sanitizer

Manufacturer
QUANZHOU BESTHOPE HOUSEHOLD PRODUCTS CO.,LTD.
Effective date
2020-09-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:30:42

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

For hand Sanitizing

WARNINGS SECTION

■For external use only
Flammable. Keep away from fire or flame
When using this product
n Keep out of eyes. In case of contact with eyes
flush thoroughly with water
■Avoid contact with open skin
1 Do not inhale or ingest
Stop use and ask a doctor
If skin iritation 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

Water,Glycerin,Butylene Glycol,
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 GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50049-105-01hand sanitizer100 in 1 CARTONGEL1002
50049-105-01hand sanitizer22.5 mL in 1 BOTTLEGEL22.52
50049-105-02hand sanitizer45 mL in 1 BOTTLEGEL452
50049-105-02hand sanitizer100 in 1 CARTONGEL1002
50049-105-03hand sanitizer60 in 1 CARTONGEL602
50049-105-03hand sanitizer75 mL in 1 BOTTLEGEL752
50049-105-04hand sanitizer187.5 mL in 1 BOTTLEGEL187.52
50049-105-04hand sanitizer24 in 1 CARTONGEL242
50049-105-05hand sanitizer375 mL in 1 BOTTLEGEL3752
50049-105-05hand sanitizer12 in 1 CARTONGEL122
50049-105-06hand sanitizer6 in 1 CARTONGEL62
50049-105-06hand sanitizer750 mL in 1 BOTTLEGEL7502
50049-105-07hand sanitizer2835 mL in 1 BOTTLEGEL28352
50049-105-07hand sanitizer4 in 1 CARTONGEL42
50049-105-08hand sanitizer3750 mL in 1 BOTTLEGEL37502
50049-105-08hand sanitizer4 in 1 CARTONGEL42
50049-105-09hand sanitizer135 mL in 1 BOTTLEGEL1352
50049-105-09hand sanitizer24 in 1 CARTONGEL242
50049-105-10hand sanitizer177.75 mL in 1 BOTTLEGEL177.752
50049-105-10hand sanitizer24 in 1 CARTONGEL242

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50049-105HAND SANITIZER (ETHYL ALCOHOL) GEL [QUANZHOU BESTHOPE HOUSEHOLD PRODUCTS CO.,LTD.]2Legacy NDC, 20 package rows20201001_b0926c19-dcb4-d24f-e053-2a95a90a674f.zip

Products#

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

DailyMed product names page 1 of 1 · 9 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
b092c72e-91be-7237-e053-2995a90ac52bb0926c19-dcb4-d24f-e053-2a95a90a674f2020-09-30WarningsExact identifier
spl id: b092c72e-91be-7237-e053-2995a90ac52b
spl set id: b0926c19-dcb4-d24f-e053-2a95a90a674f

Reported adverse events (FAERS/openFDA)#

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