DR. NATURE HUB- alcohol gel

Dr. Nature Hub by

Drug Labeling and Warnings

Dr. Nature Hub by is a Otc medication manufactured, distributed, or labeled by SHIMIZU CO., LTD., Korea Miracle People Corporation Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 70.0%

INACTIVE INGREDIENTS

Carbomer, Glycerin, Triethanolamine, Allantoin, Dexpanthenol, Dipotassium Glycyrrhizate, Lavandula Angustifolia (Lavender) Extract, Panax Ginseng Root Extract, Orange Oil, Limonene, Water

PURPOSE

ANTISEPTIC

WARNINGS

Flammable. Keep away from fire and flames.

For external use only.

When using this product Do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if if irritation or redness develops

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

Uses

■ Hand sanitizer to help reduce bacteria that potentially can cause disease.

Directions

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.

Package Label: Dr. Nature Hub (1gal)

Package Label: Dr. Nature Hub (5L)

INGREDIENTS AND APPEARANCE

DR. NATURE HUB 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76901-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	Alcohol	0.7 L  in 1 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
Glycerin (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
Allantoin (UNII: 344S277G0Z)
Dexpanthenol (UNII: 1O6C93RI7Z)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
LAVENDER OIL (UNII: ZBP1YXW0H8)
ASIAN GINSENG (UNII: CUQ3A77YXI)
Orange Oil (UNII: AKN3KSD11B)
LIMONENE, (+)- (UNII: GFD7C86Q1W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76901-020-01	3.78 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2020
2	NDC: 76901-020-02	5 L 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	part333E	05/01/2020

Labeler - SHIMIZU CO., LTD. (694646122)

Registrant - SHIMIZU CO., LTD. (694646122)

Establishment
Name	Address	ID/FEI	Business Operations
Korea Miracle People Corporation Co.,Ltd		693710617	manufacture(76901-020)