DEFENDER FOAMING HAND SANITIZER- alcohol liquid

DEFENDER Foaming Hand Sanitizer by

Drug Labeling and Warnings

DEFENDER Foaming Hand Sanitizer 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

Ethyl Alcohol 62%

Purpose

Antimicrobial

Uses

• For hand sanitizing to decrease bacteria on the skin that could cause disease.
• Recommended for repeated use.
  

Warnings

• Flammable. Keep away from fire or flame.
• For external use only
  

When using this product

avoid contact with eyes.  In case of eye contact, flush eyes with water.

Stop use and ask a doctor

irritation or redness develops or if condition persists for more than 72 hours.

Keep out of reach of children.

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

Directions

• Place enough product in your palm to thoroughly cover your hands.
• Rub hands together briskly until dry.
• Children under 6 years of age should be supervised when using this product
  

Other Information

• Store below 110 0F (43 0C)
• May discolor certain fabrics or surfaces
  

Inactive Ingredients

Water, DEA-C8-18 Perfluoroalkylethyl Phosphate, Glycerin

PRINCIPAL DISPLAY PANEL

DE Fender   SCIENTIFIC MOLECULAR TECHNOLOGIES     Foaming Hand Sanitizer   ELIMINATES 99.999% OF MOST COMMON GERMS THAT CAUSE ILLNESS    NO RINSE MOISTURIZES LEAVES SKIN SOFT     1.7 fl oz (50 ml)

Product Label

INGREDIENTS AND APPEARANCE

DEFENDER FOAMING HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42953-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42953-001-00	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/11/2012
2	NDC: 42953-001-01	550 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/11/2012
3	NDC: 42953-001-02	1000 mL in 1 BOTTLE; 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(42953-001)