FOAMING HAND SANITIZER liquid

Foaming Hand Sanitizer by

Drug Labeling and Warnings

Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Theochem Laboratories Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

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

Warnings

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 if 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:

Pour contents into the Foaming Dispenser reservoir. For first use applications, pump dispenser a few time to prime. Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

Other Information

Store below 110 °F (43 °C). May discolor certain fabrics or surfaces.

Inactive Ingredients

Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereteh-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, aloe barbadensis leaf juice.

PRINCIPAL DISPLAY PANELFOAMING HAND SANITIZER NET CONTENTS: 3.785 LITERS 

INGREDIENTS AND APPEARANCE

FOAMING HAND SANITIZER 
foaming hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68878-119
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68878-119-11	3785 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/01/2008

Labeler - Theochem Laboratories Inc (004100038)

Registrant - Theochem Laboratories Inc (004100038)

Establishment
Name	Address	ID/FEI	Business Operations
Theochem Laboratories Inc		004100038	manufacture(68878-119)