QUIK SPRAY - advanced hand sanitizing spray spray 
Cinogen Cosmetics Zhaoqing, LTD.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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QuikSpray Advanced Hand Sanitizing Spray

Drug Facts

Active Ingredients                              Purpose

Ethyl Alcohol 62 percent                   Antimicrobial

Triclosan 0.3 percent                        Antimicrobial

Uses

For hand washing to decrease bacteria on the skin,

recommended for repeated use.

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.

Directions

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

Not recommended for infants.

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

Perfume , Propylene Glycol , Tocopherol

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

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

QuikSpray24Pieces

QUIK SPRAY 
advanced hand sanitizing spray spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41900-500
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.03 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41900-500-0224 in 1 BOX
1NDC:41900-500-018 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33310/01/2009
Labeler - Cinogen Cosmetics Zhaoqing, LTD. (527929812)
Registrant - Cinogen Cosmetics Zhaoqing, LTD. (527929812)
Establishment
NameAddressID/FEIBusiness Operations
Cinogen Cosmetics Zhaoqing, LTD.527929812manufacture
Establishment
NameAddressID/FEIBusiness Operations
Nupak LLC826963550import

Revised: 9/2009
Document Id: 78ec0a6b-2382-42ff-8cb5-40d45576e022
Set id: b1a50a4a-c3ae-40fd-a735-f03021579a6e
Version: 1
Effective Time: 20090904
 
Cinogen Cosmetics Zhaoqing, LTD.