CELLAPY CLEANTECH DERMA SANITIZER-ALCOHOL-GEL- alcohol gel

Cellapy Cleantech Derma Sanitizer-alcohol-gel by

Drug Labeling and Warnings

Cellapy Cleantech Derma Sanitizer-alcohol-gel by is a Otc medication manufactured, distributed, or labeled by GM Holdings Co., Ltd, Kukbo Science Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ethanol (alcohol) 65.3 v/v%

INACTIVE INGREDIENT

glycerin, carbomer, trolamine, combination spices, water

PURPOSE

Antiseptic

instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease

instant hand antiseptic to decrease bacteria on the skin
recommended for repeated use

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.

Supervise children in the use of this product.

WARNINGS

For external use only.

Flammable, keep away from fire or flame.

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Stop use and ask a doctor if significant irritation or sensitization develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Pour a small amount into hands, spread evenly and rub into the skin

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CELLAPY CLEANTECH DERMA SANITIZER-ALCOHOL-GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69278-115
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65.3 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER 934 (UNII: Z135WT9208)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69278-115-01	25 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/04/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/04/2020

Labeler - GM Holdings Co., Ltd (688439958)

Registrant - GM Holdings Co., Ltd (688439958)

Establishment
Name	Address	ID/FEI	Business Operations
Kukbo Science Co., Ltd.		687792812	manufacture(69278-115)