Label: HAND SANITIZER BY MEDPANOL- ethanol liquid

  • Category: HUMAN OTC DRUG LABEL

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 September 9, 2020

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  • Active Ingredient

    Ethanol 69% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic

  • Uses

    Sanitizes hand to help reduce bacteria on the skin

    Recommended for repeated use

  • Warnings

    For external use only

    Keep away from Fire or Flame, Flammable

  • DO NOT USE

    Do Not Use on children under 2 months of age

    Do Not Use on open skin wounds

  • WHEN USING

    Do not use near eyes nose and mouth

    In case of contact with eyes, rinse eyes thoroughly with water

  • STOP USE

    STOP use and ask a doctor if redness, irritation or rash occurs or if condition persists for more than 72 hours

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

    If swallowed, go to your nearest hospital for immediate medical help or contact the Posion Control Center right away

  • Directions

    Place enough product onto palm to cover your hands and rub hands together until dry.
    Children under 6 years of age should be supervised with using this product.

    Do not swallow or use near eyes, nose and mouth.

  • STORAGE AND HANDLING

    Store 68-77℉ (20-25℃)

    Protect this product from excessive heat and direct sunlight

    When exposed to excessive heat 104℉/40℃, the effectiveness of the hand sanitizer will be diminished.

    May discolor some fabrics

    Harmful to wood finishes and plastics

  • Inactive ingredients

    Aloe Vera Extract, Centella Asiatica Extract, Rose Water, Allantoin, Vitamin B5, Glycerin, Hyaluronic Acid, Isopropyl Myristate, PEG 40, Fragrance, Water

  • Package Label - Principal Display Panel

    38

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER BY MEDPANOL 
    ethanol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77606-103
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL26.22 mL  in 38 mL
    Inactive Ingredients
    Ingredient NameStrength
    PEG-40 SORBITAN DIISOSTEARATE (UNII: JL4CCU7I1G)  
    ALLANTOIN (UNII: 344S277G0Z)  
    PANTOTHENIC ACID, (+/-)- (UNII: 66Y94D1203)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    SEDUM ROSEUM WHOLE (UNII: RH0WP583U3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    P-ANISIC ACID (UNII: 4SB6Y7DMM3)  
    CENTELLA ASIATICA (UNII: 7M867G6T1U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77606-103-0138 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/09/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/09/2020
    Labeler - Sun Hing Petrochemical Company Limited (662689140)
    Registrant - A03 Lab of BTS (548009541)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sun Hing Petrochemical Company Limited662689140manufacture(77606-103) , label(77606-103)
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