Genuine Hand Sanitizer

Manufacturer
GFA Production (Xiamen) Co., Ltd.
Effective date
2024-10-09
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 20:53:09

Label at a glance#

ProductGenuine Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

For hand washing to decrease bacteria on the skin.

Dosage and administration

Empty contents into palm, rub hands until gel dissipates. Recommended for repeated use.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 62%

Purpose

OTC - PURPOSE SECTION

Uses:

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Warnings:

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not use:

OTC - DO NOT USE SECTION

in eyes. In case of contact, rinse eyes thoroughly with water.

Discontinue use and consult a doctor

OTC - ASK DOCTOR SECTION

if irritation or redness develops and persists for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

Empty contents into palm, rub hands until gel dissipates.

Recommended for repeated use.

Other information:

SPL UNCLASSIFIED SECTION

Store at 15° to 25° C (59° to 77° F).

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Propylene glycol, Carbomer, Titaniumdioxide, Purified water.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50814-004GENUINE HAND SANITIZER (ETHYL ALCOHOL) CREAM [GFA PRODUCTION (XIAMEN) CO., LTD.]7Unmatched20241010_715caa22-9f9f-44c8-bf19-0ef0260ecc0e.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
50814-00450814-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
2406bbc8-88d5-b5c3-e063-6394a90af75b715caa22-9f9f-44c8-bf19-0ef0260ecc0e2024-10-09WarningsExact identifier
spl id: 2406bbc8-88d5-b5c3-e063-6394a90af75b
spl set id: 715caa22-9f9f-44c8-bf19-0ef0260ecc0e

Reported adverse events (FAERS/openFDA)#

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