DECON HAND INSTANT HAND SANITIZER- alcohol liquid

Decon Hand Instant Hand Sanitizer by

Drug Labeling and Warnings

Decon Hand Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Veltek Associates, Inc., Central Solutions Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Purpose

Antiseptic Handwash

Active Ingredients

Ethanol 64.5 (w/w)

Uses

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

Warnings

Flammable, keep away from fire or flame when using this product

For External Use Only

• Do not use in eyes.
• In case of eye contact, flush with water for 15 minutes.
• Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.
• Avoid contact with broken skin.
  

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.
  

Other Information

For Spill/Exposure Emergency Response Service in English, French and Spanish (and 23 other languages), call CARECHEM24 at 866-928-0789.

Inactive Ingredients

Acrylates/C10/30 Alkyl Acrylate Crosspolymer, EDTA, Fragrance, Glycerin, Purified Water and Tetrahydroxypropyl Ethylenediamine.

Questions?

Call 610-644-8335

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

DECON HAND INSTANT HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64307-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	64.5 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
EDETIC ACID (UNII: 9G34HU7RV0)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
EDETOL (UNII: Q4R969U9FR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64307-001-09	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/1999
2	NDC: 64307-001-10	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/1999
3	NDC: 64307-001-04	472 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/1999
4	NDC: 64307-001-06	472 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/1999
5	NDC: 64307-001-02	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/1999
6	NDC: 64307-001-05	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/1999

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/01/1999

Labeler - Veltek Associates, Inc. (108844119)

Establishment
Name	Address	ID/FEI	Business Operations
Central Solutions Inc.		007118524	manufacture(64307-001) , label(64307-001) , pack(64307-001)

Establishment
Name	Address	ID/FEI	Business Operations
Veltek Associates, Inc.		108844119	manufacture(64307-001) , pack(64307-001) , label(64307-001)