FDA.reportPublic FDA data

FA Hand Sanitizer Gel 70% (Ethanol)

Manufacturer
HLB CO.,LTD_Healthcare
Effective date
2024-02-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:11:47

Label at a glance#

ProductFA Hand Sanitizer Gel 70% (Ethanol)
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

Storage and handling

Store below 86 o F (Between 1 o C-30 o C). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

DOSAGE & ADMINISTRATION SECTION

Hand Sanitizer to help reduce bacteria on the skin.

Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only - hands

Flammable, Keep awa from fire or flame

When useing this product

OTC - WHEN USING SECTION

-do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

-avoid contact with broken skin.

-do not inhale or ingest.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

INDICATIONS & USAGE SECTION

Place enough product in your palm to thoroughly cover your hands.

Rub hands together briskly until dry.

Children under 6 years of age should be supervised when using this product.

Not recommended for infants.

Other information

STORAGE AND HANDLING SECTION

Store below 86 oF (Between 1 oC-30 oC).

May discolor certain fabrics or surfaces.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Carbormer, Fragrance, Glycerin, Triethanolamine, Water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74932-100-012024-02-22C16284748780-1f386c649-ad9b-0266-e053-dadaa90a7c1aa2f9856c-127f-2cfd-e053-2a95a90aedd6
74932-100-012023-01-30C16284748780-1f386c649-ad9b-0266-e053-dadaa90a7c1aa2f9856c-127f-2cfd-e053-2a95a90aedd6

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
74932-10074932-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT

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
1c557da5-9b30-8555-e063-6394a90ab557a2f9856c-127f-2cfd-e053-2a95a90aedd62024-07-03WarningsExact identifier
spl set id: a2f9856c-127f-2cfd-e053-2a95a90aedd6

Reported adverse events (FAERS/openFDA)#

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