DR. NATURE HUB- alcohol gel 
SHIMIZU CO., LTD.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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

PURPOSE: ANTISEPTIC

WARNINGS

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

Keep out of reach of children 

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

Uses

Uses

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

Directions

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.PRINCIPAL DISPLAY PANEL

Image of bottle

DR. NATURE HUB 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76901-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol350 mL  in 500 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76901-010-01500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/01/2020
Labeler - SHIMIZU CO., LTD. (694646122)
Registrant - SHIMIZU CO., LTD. (694646122)
Establishment
NameAddressID/FEIBusiness Operations
Korea Miracle People Corporation Co.,Ltd693710617manufacture(76901-010)

Revised: 5/2020
Document Id: 48884967-3773-43b2-af4d-14dce41521b2
Set id: 5af16956-51a6-4394-baa8-914da6eb88fb
Version: 2
Effective Time: 20200514
 
SHIMIZU CO., LTD.