ARTEMIS ALCOHOL-FREE ANTISEPTIC FOAM HAND- benzalkonium chloride soap

ARTEMIS Alcohol-Free Antiseptic Foam Hand by

Drug Labeling and Warnings

ARTEMIS Alcohol-Free Antiseptic Foam Hand by is a Otc medication manufactured, distributed, or labeled by Artemis Bio-Solutions Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

ACTIVE INGREDIENT

Active Ingredients

Benzalkonium Chloride 0.13%

PURPOSE

Purpose

Antimicrobial

Uses

• For washing hands to decrease bacteria on the skin.
• Recommended for repeated use.

WARNINGS

Warnings

• For external use only.
  

• Do not use in eyes. If contact occurs, flush eyes with water.
  

• Stop use and ask a doctor if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.
  

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

DOSAGE & ADMINISTRATION

Directions

• Pump a small amount of foam into palm of hand.
• Rub thoroughly over all surfaces of both hands for 15 seconds.
  
• Rinse with potable water.
  

INACTIVE INGREDIENT

Inactive Ingredients

Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereth-2cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

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ARTEMIS BIOSOLUTIONS

Manufactured by Artemis BioSolutions.

960 N. Industrial Dr., Ste.4 Elmhurst, IL 60126.

Made in USA.

PRINCIPAL DISPLAY PANEL

TRICLOSAN FREE


ARTEMIS
Many threats. One solution

ANTISEPTIC FOAM HAND SOAP

MOISTURIZES
LEAVES SKIN SOFT

Eliminates 99.999%
OF MOST COMMON GERMS THAT MAY CAUSE ILLNESS


Environmentally  Friendly
8.4  floz (250ml)

INGREDIENTS AND APPEARANCE

ARTEMIS ALCOHOL-FREE ANTISEPTIC FOAM HAND 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49765-410
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49765-410-08	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/24/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/24/2011

Labeler - Artemis Bio-Solutions Inc (116934417)

Establishment
Name	Address	ID/FEI	Business Operations
Artemis Bio-Solutions Inc		116934417	manufacture(49765-410)