QUASH MULTI SANITIZER- ethanol spray

QUASH MULTI SANITIZER by

Drug Labeling and Warnings

QUASH MULTI SANITIZER by is a Otc medication manufactured, distributed, or labeled by CURESCRIPT, Biostech Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

QUASH MULTI SANITIZER 
ethanol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72265-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	20.4 g  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72265-103-01	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/01/2021

Labeler - CURESCRIPT (694894509)

Registrant - CURESCRIPT (694894509)

Establishment
Name	Address	ID/FEI	Business Operations
Biostech Co., Ltd.		687294330	manufacture(72265-103)