QUASH MULTI SANITIZER- ethanol spray 
CURESCRIPT

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

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

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)

Revised: 2/2021
Document Id: d5e6a55d-98fb-49a5-ab19-51b8345b7038
Set id: 4fea42bc-b549-4c53-8b0a-321627521394
Version: 1
Effective Time: 20210209
 
CURESCRIPT