ZERO-DUST THE CLEAN HAND SANITIZER- alcohol gel

ZERO-DUST The Clean Hand Sanitizer by

Drug Labeling and Warnings

ZERO-DUST The Clean Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by MOTHER-K CO.,LTD, THE SUN CO.LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol

INACTIVE INGREDIENT

Carbomer, AminomethylPropanol, Aloe vera gel, Glycerin, Tocopherol, Butylene Glycol, EDTA, Grapefruit seed extract, Prufied Water

PURPOSE

Antiseptic

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

For the external use only

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

Take an appropriate amount on your hands and rib thoroughly to dry.

For children under 6, use only under adult supervision.

Not recommended use infacnts.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZERO-DUST THE CLEAN HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73429-0006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	700 mL  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALOE VERA WHOLE (UNII: KIZ4X2EHYX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73429-0006-1	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

Labeler - MOTHER-K CO.,LTD (689540220)

Registrant - MOTHER-K CO.,LTD (689540220)

Establishment
Name	Address	ID/FEI	Business Operations
MOTHER-K CO.,LTD		689540220	label(73429-0006)

Establishment
Name	Address	ID/FEI	Business Operations
THE SUN CO.LTD		694433104	manufacture(73429-0006)