X3 CLEAN- benzalkonium chloride aerosol, foam

X3 Clean by

Drug Labeling and Warnings

X3 Clean by is a Otc medication manufactured, distributed, or labeled by X3 Labs Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

   Antimicrobial

Use

To decrease bacteria on the skin that could cause disease.

Warnings

For external use only.

Do not use in or near eyes. In case of contact with eyes, flush thoroughly with water.

STOP USE

Stop use and ask doctor if skin irritation develops.

Keep out of reach of children

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

DOSAGE & ADMINISTRATION

Directions

Apply a small amount to palms and rub hands thoroughly until completely dry.

WARNINGS AND PRECAUTIONS

Other Information   Do not freeze.

INACTIVE INGREDIENT

Inactive Ingredients
Purified Water, Glycerin, Cocamidopropyl Betaine.

QUESTIONS

Questions? www.x3clean.com

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

X3 CLEAN 
benzalkonium chloride aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 26550-001
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)
GLYCERIN (UNII: PDC6A3C0OX)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 26550-001-12	75 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2009
2	NDC: 26550-001-14	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2009
3	NDC: 26550-001-16	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2009
4	NDC: 26550-001-18	1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product	09/01/2009
5	NDC: 26550-001-20	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/01/2009

Labeler - X3 Labs Inc. (243700361)