QUIK SPRAY- advanced hand sanitizing spray spray

Quik Spray by

Drug Labeling and Warnings

Quik Spray by is a Otc medication manufactured, distributed, or labeled by Cinogen Cosmetics Zhaoqing, LTD., Nupak LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Drug Facts

Active Ingredients                              Purpose

Ethyl Alcohol 62 percent                   Antimicrobial

Triclosan 0.3 percent                        Antimicrobial

PURPOSE

Uses

For hand washing to decrease bacteria on the skin,

recommended for repeated use.

WARNINGS

Warnings

For external use on the hands only. Flammable.

Keep away from heat and flame. Keep out if reach of children.

Stop use and ask doctor if irritation develops.

DOSAGE & ADMINISTRATION

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Not recommended for infants.

INACTIVE INGREDIENT

Aloe Barbadensis Extract , Deionized Water ,  Hydroxyehylcellulose , PEG  40 Hydrogenated Castor Oil ,

Perfume , Propylene Glycol , Tocopherol

DESCRIPTION

Net Wt 8mL 0.27 FL OZ Made in China

Dist by Nupak, LLC 5823 Bowen Daniek Dr. 1601 Tampa FL 33616 1 888 988 7232

PRINCIPAL DISPLAY PANEL

6 Hour Germ Protection

QuikSpray

90 plus sprays

Advanced Hand Sanitizing Spray

www.myquikspray.net

Contains Aloes Vera and Vitamin E

Kills 99.99 percent of germs

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

QUIK SPRAY 
advanced hand sanitizing spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41900-500
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL  in 1 mL
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.03 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
HYDROXYETHYL CELLULOSE (140 CPS AT 5%) (UNII: 8136Y38GY5)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41900-500-02	24 in 1 BOX
1	NDC: 41900-500-01	8 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	10/01/2009

Labeler - Cinogen Cosmetics Zhaoqing, LTD. (527929812)

Registrant - Cinogen Cosmetics Zhaoqing, LTD. (527929812)

Establishment
Name	Address	ID/FEI	Business Operations
Cinogen Cosmetics Zhaoqing, LTD.		527929812	manufacture

Establishment
Name	Address	ID/FEI	Business Operations
Nupak LLC		826963550	import