QC 8OZ INSTANT HAND SANITIZER (ORIGINAL)- alcohol gel

QC 8OZ INSTANT HAND SANITIZER (ORIGINAL) by

Drug Labeling and Warnings

QC 8OZ INSTANT HAND SANITIZER (ORIGINAL) by is a Otc medication manufactured, distributed, or labeled by Ningbo Liyuan Daily Chemical Products Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts Medicinal Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Non-Medicinal

Water, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Parfum, Propylene Glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate

Features

• To decrease bacteria on the skin that could cause disease.
• Recommended for repeated use.
• Use anywhere without water.

Directions

Wet hands thoroughly with product and rub until dry without wiping.
For children under 6, use only under adult supervision.
Not recommended for infants.

Warning

• For external use only-hands
• Flammable, keep away from heat and flame
• Discontinue if skin becomes irritated and ask a doctor

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Posion Control Center immediately.

When using this product

• Keep out of eys. In case of contact with eyes, flush thoroughly with water.
• Do not inhale or ingest.
• Avoid contact with broken skin.

This product was not tested on animals

Other information

• Do not store above 105℉.
• May discolor some fabrics.
• Harmful to wood finishes and plastics.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

QC 8OZ INSTANT HAND SANITIZER (ORIGINAL) 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76176-035
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	36 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76176-035-01	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/09/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/09/2017

Labeler - Ningbo Liyuan Daily Chemical Products Co., Ltd. (530766098)

Registrant - Ningbo Liyuan Daily Chemical Products Co., Ltd. (530766098)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Liyuan Daily Chemical Products Co., Ltd.		530766098	manufacture(76176-035)