Hand Sanitizer

Manufacturer
GFA Production (Xiamen) Co., Ltd.
Effective date
2024-10-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:53:02

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

For handwashing to decrease bacteria on the skin Recommended for repeated use.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Storage and handling

Store between 15-25°C (59 to 77°F) o

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 62 v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on the skin
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame

For external use only.

SPL UNCLASSIFIED SECTION

Do not use

OTC - DO NOT USE SECTION

  • in the eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation or redness develop
  • condition 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

  • Wet hands thoroughly with product and allow to dry without wiping.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-25°C (59 to 77°F) o

Inactive Igredients

INACTIVE INGREDIENT SECTION

Carbomer, propylene glycol, purified water, titanium dioxide

​Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50814-050HAND SANITIZER (ALCOHOL) GEL [GFA PRODUCTION (XIAMEN) CO., LTD.]3Legacy NDC20241011_9dd76719-03d8-4dae-8049-262ce31032fd.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50814-05050814-050-02

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 · Source PDF

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
2408c0eb-8948-9dac-e063-6394a90afc6f9dd76719-03d8-4dae-8049-262ce31032fd2024-10-09WarningsExact identifier
spl id: 2408c0eb-8948-9dac-e063-6394a90afc6f
spl set id: 9dd76719-03d8-4dae-8049-262ce31032fd

Reported adverse events (FAERS/openFDA)#

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