DEFENDER ANTISEPTIC FOAM HAND SANITIZER ALCOHOL-FREE- benzalkonium chloride liquid

DEFENDER Antiseptic Foam Hand Sanitizer Alcohol-Free by

Drug Labeling and Warnings

DEFENDER Antiseptic Foam Hand Sanitizer Alcohol-Free by is a Otc medication manufactured, distributed, or labeled by Scientific Molecular Technologies. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

• For hand sanitizing to decrease bacteria on the skin.
• Recommended for repeated use.
  

Warnings

• For external use only.
  

Do not use in eyes

if contact occurs, flush eyes with water.

Stop use and ask a doctor

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.

Directions

• Pump a small amount of foam into palm of hand.
• Wet hands thoroughly with product and allow to dry without wiping.
• Rub hands together briskly until dry.
  

Inactive Ingredients

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

PRINCIPAL DISPLAY PANEL

DE Fender  SCIENTIFIC MOLECULAR TECHNOLOGIES    ANTISEPTIC FOAM  Hand Sanitizer  ALCOHOL-FREE    ELIMINATES 99.999% OF MOST COMMON GERMS THAT CAUSES ILLNESS   NO RINSE MOISTURIZES LEAVES SKIN SOFT   EFFECTIVE AGAINST STAPH, MRSA, VRE, NOROVIRUS   1.7 fl oz (50 ml)

Product Label

INGREDIENTS AND APPEARANCE

DEFENDER ANTISEPTIC FOAM HAND SANITIZER ALCOHOL-FREE 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42953-002
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: 42953-002-00	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/11/2012
2	NDC: 42953-002-01	550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/11/2012
3	NDC: 42953-002-02	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/11/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/11/2012

Labeler - Scientific Molecular Technologies (028159474)

Establishment
Name	Address	ID/FEI	Business Operations
Artemis Bio-Solutions Inc.		116934417	manufacture(42953-002)