Label: DR. NATURE HUB- alcohol gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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.

Drug Label Information

Updated May 14, 2020

If you are a consumer or patient please visit this version.

  • 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

  • INGREDIENTS AND APPEARANCE
    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)