KUNDAL PURE AND SAFE POCKET PERFUME HAND SANITIZER MIST HERB MINT- alcohol liquid

KUNDAL PURE and SAFE POCKET PERFUME HAND SANITIZER MIST HERB MINT by

Drug Labeling and Warnings

KUNDAL PURE and SAFE POCKET PERFUME HAND SANITIZER MIST HERB MINT by is a Otc medication manufactured, distributed, or labeled by THESKINFACTORY Co., Ltd., WHAIN COSMETIC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ethanol

INACTIVE INGREDIENT

Water, Butylene Glycol, Glycerin, Sodium Hyaluronate, Camellia Sinensis Leaf Extract, Artemisia Princeps Extract, fragrance

PURPOSE

Antiseptic

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

Put enough product in your palm to thoroughly cover your hands.

Rub hands together briskly until dry.

Children under 6 years of age should be supervised when using 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

For external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KUNDAL PURE AND SAFE POCKET PERFUME HAND SANITIZER MIST HERB MINT 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74773-0032
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74773-0032-1	18 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/09/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/09/2020

Labeler - THESKINFACTORY Co., Ltd. (694804099)

Registrant - THESKINFACTORY Co., Ltd. (694804099)

Establishment
Name	Address	ID/FEI	Business Operations
WHAIN COSMETIC		557837595	manufacture(74773-0032)

Establishment
Name	Address	ID/FEI	Business Operations
THESKINFACTORY Co., Ltd.		694804099	label(74773-0032)