NOXYDERM- benzalkonium chloride liquid

NOxyDERM by

Drug Labeling and Warnings

NOxyDERM by is a Otc medication manufactured, distributed, or labeled by NOxy Health Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

• Active Ingredient: Purpose
• Benzalkonium Chloride 0.13%: First Aid Antiseptic

Purpose

Purpose

First aid antiseptic

Uses: first aid to help prevent infection in minor:

• cuts
• scrapes
• burns

Do not use

Do not use

• in the eyes
• over large areas of the body
• longer than 1 week unless directed by a doctor

Ask a doctor before use if you have

• deep or pucture wounds, animal bites, or serious burns

Warnings For external use only

Warnings

For external use only

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact Poison Control right away

Instructions for use

Directions

• Clean the affected area
• Apply a small amount of this product on the area 1 to 3 times daily
• May be covered with a sterile bandage
• If bandaged, let dry first

Other safety information

Store at room temperature

Dosage

• Apply a small amount of this product on the area 1 to 3 times daily

Inactive ingredients

Sodium Nitrite

CoCo Betaine

Deionized Water

Citric Acid

INDICATIONS & USAGE

Directions:

• Clean the affected area
• Apply a small amount of this product on the area 1 to 3 times daily
• May be covered with a sterile bandage
• If bandaged, let dry first

Warnings

Warnings:

For external use only

Questions

Questions? call 1-888-585-4120

NOxyDERM

INGREDIENTS AND APPEARANCE

NOXYDERM 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83823-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
COCO-BETAINE (UNII: 03DH2IZ3FY)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM NITRITE (UNII: M0KG633D4F)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83823-001-01	100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/05/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	01/05/2024

Labeler - NOxy Health Products (119031427)