FDA.reportPublic FDA data

Moisturizing Hand Sanitizer Gel

Manufacturer
IMEI CHEMICAL ENTERPRISE LTD.
Effective date
2020-07-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:23:30

Label at a glance#

ProductMoisturizing Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

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

Storage and handling

Do not store above 105F/40C. Store in a cool dry place, away for 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

Be used on the hands without water as a cleansing

Warnings

WARNINGS SECTION

For external use only, do not inhale or ingest

Flammable keep away from fireor flame or direct sunlight

OTC - WHEN USING SECTION

When using the product keep out of eyes. In case of eye contact, flush 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, spray product on your palm to thoroughly cover your hand, rub hands together for 10 to 15 seconds until dry. Use as needed.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back LabelsFront and Back Labels1000 mL NDC: 77660-202-01

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
77660-20277660-202-01

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

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
c706344a-d9e1-7bf9-e053-2a95a90af269a96aa8ec-5981-6e34-e053-2995a90a9b522021-07-13WarningsExact identifier
spl set id: a96aa8ec-5981-6e34-e053-2995a90a9b52

Reported adverse events (FAERS/openFDA)#

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