FDA.reportPublic FDA data

THE CLEAN LAB HAND SANITIZER

Manufacturer
FEEL COSMETIC KOREA CO., LTD
Effective date
2020-05-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:31:08

Label at a glance#

ProductTHE CLEAN LAB HAND SANITIZER
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Squeeze a dime-sized drop on hands and rub together. Allow to dry without wiping off.

Storage and handling

Precautions for storage and handling.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Directions

DOSAGE & ADMINISTRATION SECTION

Squeeze a dime-sized drop on hands and rub together. Allow to dry without wiping off.

Directions

INDICATIONS & USAGE SECTION

Squeeze a dime-sized drop on hands and rub together. Allow to dry without wiping off.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Chamaecyparis Obtusa Leaf Extract, Butylene Glycol, 1,2-Hexanediol, Tromethamine, Citrus Limon (Lemon) Peel Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Tocopheryl Acetate, Panthenol, Pantolactone

Precautions When Using

OTC - ASK DOCTOR SECTION

When using cosmetics or after use, consult a specialist if you have any abnormal symtoms such as red spots, swelling or itching, or side effects caused by direct sunlight.

Precautions When Using

OTC - DO NOT USE SECTION

Do not use on wounded areas.

Precautions When Using

STORAGE AND HANDLING SECTION

Precautions for storage and handling.

Precautions When Using

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

Precautions When Using

WARNINGS SECTION

Store away from direct sunlight.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500ml NDC: 74454-320-01 Label500ml NDC: 74454-320-01 Label

300ml NDC: 74454-320-02300ml NDC: 74454-320-02

500ml NDC: 74454-320-03 Label500ml NDC: 74454-320-03 Label

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74454-32074454-320-01, 74454-320-02, 74454-320-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TEA TREE OILVIF565UC2GIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
LEMON OILI9GRO824LLIACT
PANTHENOLWV9CM0O67ZIACT
PANTOLACTONE, (R)-J288D7O0JSIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
TROMETHAMINE023C2WHX2VIACT
CHAMAECYPARIS OBTUSA LEAF7OL154J5XBIACT

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
b71e1354-29b5-fa3a-e053-2a95a90a1d4aa4487d8d-6892-7b7c-e053-2a95a90a1aa62020-12-23WarningsExact identifier
spl set id: a4487d8d-6892-7b7c-e053-2a95a90a1aa6

Reported adverse events (FAERS/openFDA)#

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