FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
BRIDGE TOP INTERNATIONAL ENTERPRISES CO., LTD.
Effective date
2022-01-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:18:58

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

After washing your hand, squeeze product on your palm to thoroughly cover your hands, rub together for 10 to 15 seconds until dry. Use as needed.

Storage and handling

Do not store above 105˚F/40˚C. Store in a cool dry place, away from direct sunlight

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Squeeze on hand and rub without water as a cleansing

Warnings

WARNINGS SECTION

For external use only, do not inhale or ingest.

Flammable, keep away from fire or flame or direct sunlight.

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of eye contact, rinse thoroughly with water and get medical help.

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

For children under 6, use only under adult supervision. Keep out of reach of children.

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

Directions

DOSAGE & ADMINISTRATION SECTION

After washing your hand, squeeze product on your palm to thoroughly cover your hands, rub together for 10 to 15 seconds until dry. Use as needed.

Other information

STORAGE AND HANDLING SECTION

Do not store above 105˚F/40˚C. Store in a cool dry place, away from direct sunlight

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Triethanolamine, Polysorbate 20, Tocopheryl Acetate, Hydrolyzed Hyaluronic Acid

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box LabelsBox Labels2 mL NDC: 79629-001-03

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79629-00179629-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER 1342809Y72KV36IACT
ECAMSULE DITRIETHANOLAMINE078Q44I6CDIACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
ALCOHOL3K9958V90MACTIB
POLYSORBATE 207T1F30V5YHIACT
HYALURONIC ACIDS270N0TRQYIACT
WATER059QF0KO0RIACT

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
e393c251-9139-7f62-e053-2a95a90a3fdeaa9a7a42-0dbd-70ab-e053-2995a90ac7ab2022-07-11WarningsExact identifier
spl set id: aa9a7a42-0dbd-70ab-e053-2995a90ac7ab

Reported adverse events (FAERS/openFDA)#

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