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

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 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 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 only under adult supervision.

STORAGE AND HANDLING

Other Information
Do not store above 105 degree F
May discolor some fabrics.

INACTIVE INGREDIENT

Inactive Ingredients

Water, PEG 40 Hydrogenated Castor Oil , Acrylic Polymer,

Aloe Barbadensis, Fragrance, Triethanolamine, Tocopheryl Acetate

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.

DESCRIPTION

Distributed by

NUPAK LLC

5823 Bowen Daniel Dr

Tampa, FL 3361

Made in China

QUESTIONS

Questions

1 888 988 7232

www.myquikspray.net

PRINCIPAL DISPLAY PANEL

New

Quik Gel

Advanced Hand Sanitizing Gel Singles

6 Hour Germ Protection

Aloe Vera and Vitamin E

Kills 99.99 percent of Germs

NET WT .045 oz 1.28g

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: 41900-200
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41900-200-02	10 in 1 BAG
1	NDC: 41900-200-01	1.28 g in 1 PACKET

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