DEPHYZE ANTISEPTIC FOAM HAND SANITIZER  - benzalkonium chloride spray 
MicroPure Solutions, LLC dba Tionicon

DepHyze Alcohol Free Antiseptic Foam Hand Sanitizer

Drug Facts

Active Ingredient                                             Purpose

Benzalkonium Chloride 0.13 percent            Antiseptic

Uses:

For handwashing to decrease bacteria on the skin. Recommended for repeated use.

Warnings:

For external use only. Do not use in the eyes.

Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a  doctor.

Stop use and ask  a doctor if side effects occur. You may report side effects to FDA at 1-800-FDA-1088.

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

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

Behentrimonium Chloride, Citric Acid, Dihydroxyethyl Cocamide Oxide, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Fragrance, Glycereth-2 Cocoate, Glycerin, Potassium Carbonate, Water.

No Rinse -  Leaves Skin Soft

Exp. Date 3 2001

DepHyze
Alcohol Free
Antiseptic Foam
Hand Sanitizer

Effective to 99.999 percent on germs that cause illnesses

Net Weight 1.7 fl oz (50 mL)

Tionicon
www.tionicon.com
Aurora, CO
Made in U.S.A.

DEPHYZE ANTISEPTIC FOAM HAND SANITIZER  benzalkonium chloride  spray

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 49765-100 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.13 mL  in 100 mL

Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE   GLYCERIN   POTASH   WATER

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 49765-100-10 50 mL In 1 BOTTLE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	11/01/2023

Labeler - MicroPure Solutions, LLC dba Tionicon (805764508)

Registrant - MicroPure Solutions, LLC dba Tionicon (805764508)

Establishment
Name	Address	ID/FEI	Operations
MicroPure Solutions, LLC dba Tionicon		805764508	manufacture

Revised: 12/2009MicroPure Solutions, LLC dba Tionicon