QUIK GEL- advanced hand sanitizing gel gel

Quik Gel by

Drug Labeling and Warnings

Quik Gel 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

Active Ingredients                           Purpose

Ethyl Alcohol 62 percent                 Antimicrobial

Triclosan 0.3 percent                      Antimicrobial                

PURPOSE

Uses   For hand washing to decrease bacteria on the skin that may cause disease.

Recommended for repeat use.

WARNINGS

Warning Directions   

For external use only. Flammable. Keep away from heat and flame. When using this product, keep out of eyes.

In case of contact with eyes, flush thoroughly with water.

STOP USE

Stop use and ask doctor if irritation develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

INDICATIONS & USAGE

Directions

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

For children under 6, use only under adult supervision.

USER SAFETY WARNINGS

Other Information

Do not store above 105 degrees F. May discolor some fabrics.

INACTIVE INGREDIENT

Inactive Ingredients

Water, PEG-40 Hydrogenated Castor Oil, Acrylic Polymer, Aloe Barbadensis, Acrylic Polymer, Fragrance, Triethanolamine, Tocopheryl Acetate

QUESTIONS

Questions? 1-888-988-7232

www.myquikspray.net

INFORMATION FOR PATIENTS

6 Hour Protection: Hands will be protected from germs for over 6 hours as long as hands are not washed with soap and water during that period of time.

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

QUIK GEL 
advanced hand sanitizing gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41900-100
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
WATER (UNII: 059QF0KO0R)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41900-100-01	59 mL in 1 BOTTLE, SPRAY
2	NDC: 41900-100-02	236 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	09/05/2009

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