PUR USA HAND MIST REFRESHING HAND SANITIZER- alcohol liquid

PUR USA Hand Mist Refreshing Hand Sanitizer by

Drug Labeling and Warnings

PUR USA Hand Mist Refreshing Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by MESO PHARM CO LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

alcohol

INACTIVE INGREDIENT

Water, Propylene Glycol, Dipropylene Glycol, Glycerin, Butylene Glycol, Sodium Hyaluronate, Hydrolyzed Sodium Hyaluronate, Hyaluronic Acid, Sodium Hyaluronate Crosspolymer, Hydrolyzed Hyaluronic Acid, Centella Asiatica Extract, Aloe Barbadensis Leaf Juice, Brassica Oleracea Acephala Leaf Extract, Persea Gratissima (Avocado) Fruit Extract, Apium Graveolens (Celery) Extract, 1,2-Hexanediol

PURPOSE

Sterilization of hands and skin

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.

Supervise children in the use of this product.

WARNINGS

■ Flammable. Keep away from fire or flame.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PUR USA HAND MIST REFRESHING HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77098-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77098-0002-1	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2020

Labeler - MESO PHARM CO LTD (695708527)

Registrant - MESO PHARM CO LTD (695708527)

Establishment
Name	Address	ID/FEI	Business Operations
MESO PHARM CO LTD		695708527	manufacture(77098-0002)