NATURE HAND TOUCH SANITIZER LIQUID (ETHANOL) 70%- alcohol liquid

Nature Hand Touch Sanitizer Liquid (ethanol) 70% by

Drug Labeling and Warnings

Nature Hand Touch Sanitizer Liquid (ethanol) 70% by is a Otc medication manufactured, distributed, or labeled by Dai Kyoung Pharmaceutic Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol (Ethanol)

INACTIVE INGREDIENT

Polysorbate 20, Gylcerin, cherry Fragrance, Sodium Hyaluronate, Collagen, Water

PURPOSE

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Place enough product on hands to cover all surfaces. Rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing.

WARNINGS

For external use only. Flammable. Keep away from heat or flame.

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

NATURE HAND TOUCH SANITIZER LIQUID (ETHANOL) 70% 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74279-0020
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74279-0020-1	750 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/30/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/30/2021

Labeler - Dai Kyoung Pharmaceutic Co.,Ltd. (695045937)

Registrant - Dai Kyoung Pharmaceutic Co.,Ltd. (695045937)

Establishment
Name	Address	ID/FEI	Business Operations
Dai Kyoung Pharmaceutic Co.,Ltd.		695045937	manufacture(74279-0020) , label(74279-0020) , pack(74279-0020)