Label: NEXSENSE LIQUID HAND SANITIZER MOISTURIZING WITH ALOE- alcohol solution

  • 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 June 19, 2020

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  • Active Ingredient(s)

    Ethyl Alcohol 62% v/v

  • Purpose

    Antiseptic

  • Use

    Hand sanitizer to help decrease bacteria on the skin

    Recommended for repeated use

  • Warnings

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

    Do not apply around eyes or use in ears or mouth

    Stop use and contact a doctor if redness or irritation develop or persist for more than 72 hours

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.

  • Directions

    • Pump as needed into your palms and thoroughly spead on both hands
    • rub into skin until dry
  • Other information

    • Store at room temperature no higher than 45C (115F) and under shade
    • Keep in closed containers and free from direct sunlight 
  • Inactive ingredients

    Water, Glycerol, Aminomethyl propanol, Aloe Vera gel, Vitamin E, Carbomer, Frangrance

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    NEXSENSE LIQUID HAND SANITIZER MOISTURIZING WITH ALOE 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52989-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER 934 (UNII: Z135WT9208)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    ALOE VERA WHOLE (UNII: KIZ4X2EHYX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52989-003-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product06/19/2020
    2NDC:52989-003-02250 mL in 1 BOTTLE; Type 0: Not a Combination Product06/19/2020
    3NDC:52989-003-03500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/19/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/19/2020
    Labeler - Taizhou Yadai Daily-Use Co., Ltd. (529899639)
    Establishment
    NameAddressID/FEIBusiness Operations
    Taizhou Yadai Daily-Use Co., Ltd.529899639manufacture(52989-003)
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