FRESHORIZE ALCOHOL FREE FOAMING HAND SANITIZER- benzalkonium chloride lotion

Freshorize by

Drug Labeling and Warnings

Freshorize by is a Otc medication manufactured, distributed, or labeled by Freshorize, Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

0.13% Benzylkonium Chloride

Requires no water or towels.  Apply small amount to hands and rub lightly until dry.

WARNINGS

Safety: Avoid contact with  Eyes, should this occur  rinse immediately with clean warm water.

Caution: Use on hands only.



 

Display of package label.

Picture of Package Label

Keep out of reach of children

Keep out of reach of children

Purpose

Kills 99.9% Bacteria

DOSAGE & ADMINISTRATION

Requires no water or towels.

Apply small amount to hands and rub lightly until dry.

INACTIVE INGREDIENT

Aqua, Polysorbate 40, Aloe Barbadensis, Parfum

INGREDIENTS AND APPEARANCE

FRESHORIZE  ALCOHOL FREE FOAMING HAND SANITIZER
benzalkonium chloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52305-300
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	.364 g  in 280 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
POLYSORBATE 40 (UNII: STI11B5A2X)
ALOE VERA FLOWER (UNII: 575DY8C1ER)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52305-300-20	280 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2010

Labeler - Freshorize, Ltd. (424168503)

Registrant - Freshorize, Ltd. (424168503)

Establishment
Name	Address	ID/FEI	Business Operations
Freshorize, Ltd.		424168503	manufacture