Label: QUASH MULTI SANITIZER- ethanol spray

  • 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 February 9, 2021

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    Ethanol 68% (w/w)

  • INACTIVE INGREDIENTS

    Water, Glycerin,Allantoin,Water,Fragrance,Aloe Extract, TEA TREE OIL,Sodium Hyaluronate,Centella asiatica Extract,Eucalyptus Oil

  • PURPOSE

    Antiseptic

  • WARNINGS

    For external use only-hands

    Flammable. Keep away from heat and flame.

    When using this product ■ Keep out of eyes. In case of contact with eyes, flush thoroughly with water. ■ Avoid contact with broken skin. ■ Do not inhale or ingest.

    Stop use and ask a doctor if skin irritation or rash develops.

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

  • KEEP OUT OF REACH OF CHILDREN

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

  • Uses

    ■ Hand sanitizer to decrease bacteria on the skin that could cause disease

  • Directions

    ■ Spray enough product in your hands to thoroughly cover your hands.
    ■ rub hands together briskly until dry
    ■ Supervise children under 6 years of age when using this product to avoid swallowing.
    ■ no recommended for infants

  • Other Information

    ■ Store between 15-30C (59-86F)
    ■ Avoid freezing and excessive heat above 40C (104F)
    ■ May discolor certain fabrics or surfaces

  • QUESTIONS

    www.getquash.com
    tel) +820218117395

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    QUASH MULTI SANITIZER 
    ethanol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72265-103
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL20.4 g  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Allantoin (UNII: 344S277G0Z)  
    Aloe (UNII: V5VD430YW9)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)  
    Eucalyptus Oil (UNII: 2R04ONI662)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72265-103-0130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A02/01/2021
    Labeler - CURESCRIPT (694894509)
    Registrant - CURESCRIPT (694894509)
    Establishment
    NameAddressID/FEIBusiness Operations
    Biostech Co., Ltd.687294330manufacture(72265-103)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!