FDA.reportPublic FDA data

Detox Perfect Hand Gel

Manufacturer
HUMEX,INC. | MESO PHARM CO., LTD
Effective date
2020-05-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:30:35

Label at a glance#

ProductDetox Perfect Hand Gel
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

▪ Place enough product in your palm thoroughly cover your hands ▪ Rub hands together and pat until absorbed ▪ Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Drug Facts Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

label showing drug factslabel showing drug facts

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.
This product is intended for external use only
When using this product, do not use in or near the eyes. In case of contact, rinse with water to remove.
Discontinue use if irritation or redness develops.If condition persists for more than 72 hours, consult a doctor.

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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

▪ Place enough product in your palm thoroughly cover your hands
▪ Rub hands together and pat until absorbed
▪ Children under 6 years of age should be supervised when using this product.

Other Information

OTHER SAFETY INFORMATION

▪ Store below 110ºF (43ºC)
▪ May discolor certain fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Dipropylene Glycol, Glycerin, Butylene Glycol, Sodium Hyaluronate, Hyaluronic Acid, Centella Asiatica Extract, Aloe Vera Leaf, Kale Leaf Extract, Avocado Fruit Extract, Celery Extract, Homopolymer, Hexacosyl Glycol, Trolamine

USE

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Use

OTC - PURPOSE SECTION

Hand sanitizer to help reduce bacteria on the skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70ml NDC: 76344-8004-1

label with drug factslabel with drug facts

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76344-800476344-8004-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYALURONATE SODIUMYSE9PPT4THIACT
CELERY44IDY6DTKXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALOE VERA LEAFZY81Z83H0XIACT
HEXACOSYL GLYCOLULV0C76D5HIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
TROLAMINE9O3K93S3TKIACT
AVOCADOSDS87L369FIACT
CENTELLA ASIATICA7M867G6T1UIACT
KALE0Y3L4J38H1IACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
DIPROPYLENE GLYCOLE107L85C40IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
HYALURONIC ACIDS270N0TRQYIACT

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
d57ede2b-2ac0-b4ea-e053-2a95a90a98e2a52a8247-998b-37bc-e053-2a95a90a21072022-01-13WarningsExact identifier
spl set id: a52a8247-998b-37bc-e053-2a95a90a2107

Reported adverse events (FAERS/openFDA)#

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