QUASH MULTI SANITIZING TISSUE- alcohol cloth

QUASH MULTI SANITIZING TISSUE by

Drug Labeling and Warnings

QUASH MULTI SANITIZING TISSUE 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

Alcohol 54.7% (v/v)

INACTIVE INGREDIENTS

Water,Glycerin,Sodium Benzoate,PEG-60 Hydrogenated Castor Oil ,Fragrance,Citric acid,Menthol,1,2-Hexanediol,Poloxamer 184,PEG-7 Glyceryl Cocoate,Aloe Barbadensis Leaf Extract,Thymus Vulgaris (Thyme) Extract,Sophora Flavescens Root Extract,Sodium Hyaluronate,Cocamidopropyl Betaine,Butylene Glycol,Sodium Chloride

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

■ Help decrease bacteria on the hands

Directions

■ Rive the seal
■ Pull out the wet tissue towel through small opening
■ Rub thoroughly over all surfaces of both hands with the we wipes.
■ Supervise children under 6 years of age when using this product to avoid swallowing.

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 SANITIZING TISSUE 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72265-104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.54

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Sodium Benzoate (UNII: OJ245FE5EU)
PEG-60 Hydrogenated Castor Oil (UNII: 02NG325BQG)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
Menthol (UNII: L7T10EIP3A)
1,2-Hexanediol (UNII: TR046Y3K1G)
POLOXAMER 184 (UNII: BIS92ZSF57)
PEG-7 Glyceryl Cocoate (UNII: VNX7251543)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
THYME (UNII: CW657OBU4N)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Butylene Glycol (UNII: 3XUS85K0RA)
Sodium Chloride (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72265-104-01	20 in 1 PACKET; 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(72265-104)