FDA.reportPublic FDA data

Moisturizing Hand Sanitizer

Manufacturer
IMEI CHEMICAL ENTERPRISE LTD.
Effective date
2020-05-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:29:14

Label at a glance#

ProductMoisturizing Hand Sanitizer
Active ingredientALCOHOL
Label structure10 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: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Be used on the hands without water as a cleansing

OTC - WHEN USING SECTION

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

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

Stop use and ask a doctor if skin irritation develops.

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

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, Hydrolyzed Jojoba Esters, Glycerin Metaleuca Alternifolia (Tea Tree) Leaf Oil, Citrus Aurantium Bergania (Bergamot) Fruit Oil, Eucalyptus Globulus Leaf Oil, Hydrolyzed Hyaluronic Acid

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back LabelsFront and Back Labels100 mL NDC: 77660-201-10

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77660-20177660-201-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
EUCALYPTUS OIL2R04ONI662IACT
HYALURONIC ACIDS270N0TRQYIACT
CITRUS AURANTIUM FRUIT OIL59JDQ5VT0TIACT
HYDROLYZED JOJOBA ESTERS (ACID FORM)UDR641JW8WIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
TEA TREE OILVIF565UC2GIACT

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
c7064805-3ce3-8061-e053-2995a90ace9da66fe847-1ec0-4c1b-e053-2995a90aa7fa2021-07-13WarningsExact identifier
spl set id: a66fe847-1ec0-4c1b-e053-2995a90aa7fa

Reported adverse events (FAERS/openFDA)#

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