NATIONAL UNIVERSITY HAND SANITIZER- alcohol gel

National University Hand Sanitizer by

Drug Labeling and Warnings

National University Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Zhejiang Ounuo Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol     .................... 75%         

PURPOSE

Antiseptic

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use.

WARNINGS

For external use only: hands
Flammable. Keep away from heat or flame.

When using this products

• 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 using and ask a doctor if irritation develops.

Other information

• do not store above 105℉
• may discolor some fabrics
• harmful to wood finishes and plastics

DOSAGE & ADMINISTRATION

• Wet hands thoroughly with product and allow to dry without wiping.
• for children under 6, use only under adult supervision
• not recommended for infants

INACTIVE INGREDIENT

Water (aqua), propylene glycol, Glycerin, acrylates/c10-30 alkyl acrylate crosspolymer, aminomethyl Propanol, fragrance (parfum).

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NATIONAL UNIVERSITY HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75531-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	alcohol	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75531-012-01	100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/15/2020

Labeler - Zhejiang Ounuo Cosmetics Co., Ltd. (551868984)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Ounuo Cosmetics Co., Ltd.		551868984	manufacture(75531-012)