Quik Gel description, usages, side effects, indications, overdosage, supplying and lots more!

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Quik Gel

Cinogen Cosmetics Zhaoqing, LTD.
Cinogen Cosmetics Zhaoqing, LTD.

Quik Gel Advanced Hand Sanitizing Gel




FULL PRESCRIBING INFORMATION

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.

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. If swallowed, get medical help or contact a Poison Control Center immediately.

Uses

Directions

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

For children under 6, use only under adult supervision.

Other Information

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

Inactive Ingredients

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

Questions? 1-888-988-7232

www.myquikspray.net

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.

Quik Gel

Quik Gel

Quik Gel

Advanced Hand Sanitizing Gel GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41900-100
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALCOHOL ALCOHOL 0.62 mL
TRICLOSAN TRICLOSAN 0.03 mL

Inactive Ingredients

Ingredient Name Strength
water
POLYOXYL 40 HYDROGENATED CASTOR OIL
Aloe Vera Leaf
TROLAMINE
ALPHA-TOCOPHEROL ACETATE
CARBOMER HOMOPOLYMER TYPE C

Packaging

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

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part333 2009-09-05


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