WOUND WASH ANTISEPTIC SALINE WITH BENZALKONIUM CHLORIDE aerosol, spray

Wound Wash Antiseptic Saline with Benzalkonium Chloride by

Drug Labeling and Warnings

Wound Wash Antiseptic Saline with Benzalkonium Chloride by is a Otc medication manufactured, distributed, or labeled by NeilMed Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Dosage and Administration

Before use, spray a short stream in the air or on intact skin to test spray pattern and to clear nozzle.

To dispense, aim nozzle at the affected area and spray from a distance of 2 to 4 inches, or as is comfortable.

Cover with clear cap after each use

Warnings

Do not use on burn injuries. Do not use in body orifices, ear canals, eyes or mouth.

Not for injection.

For individual use only.

Apply as needed. Consult a healthcare professional for continued wound care management and for use on children younger than 2 years of age.

Inactive Ingredients

USP Grade Water, USP Sodium Chloride (9mg/mL)

OTC Active Ingredient

Benzalkonium Chloride 0.13%

Indications and Usage

First Aid Antiseptic

First aid to cleanse minor cuts, wounds and scrapes

OTC- Purpose

First aid to cleanse minor cuts, wounds and scrapes

OTC- Keep Out of Reach of Children

Keep out of reach of children.

Wound Wash Antiseptic Sterile Saline with Benzalkonium Chloride, 75 mL

INGREDIENTS AND APPEARANCE

WOUND WASH ANTISEPTIC SALINE WITH BENZALKONIUM CHLORIDE 
wound wash antiseptic saline with benzalkonium chloride aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 13709-235
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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	9 mg  in 1 mL
WATER (UNII: 059QF0KO0R)	89.7 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 13709-235-11	75 mL in 1 CAN; Type 0: Not a Combination Product	01/02/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/02/2017

Labeler - NeilMed Pharmaceuticals, Inc. (799295915)