Drugplain

NOxyDERM .038 g/29.5mL

Benzalkonium Chloride · LIQUID · NOxy Health Products

No Recall History
Plain English

NOxyDERM is a liquid containing benzalkonium chloride at .038 g/29.5mL, taken topical. Manufactured by NOxy Health Products.

Key Facts

Brand Name
NOxyDERM
Generic Name
Benzalkonium Chloride
NDC Code (Product)
83823-002
Manufacturer
NOxy Health Products
Strength
.038 g/29.5mL
Dosage Form
LIQUID
Route
TOPICAL
Marketing Status
Application #
M003
Marketing Start
09/30/2024

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective126 reports
drug hypersensitivity118 reports
condition aggravated114 reports
therapy non-responder113 reports
arthralgia112 reports
musculoskeletal stiffness111 reports
pain in extremity111 reports
infection110 reports
hepatotoxicity108 reports
musculoskeletal pain108 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

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

Dosage & Administration

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

Warnings

Warnings Warnings: For external use only

Frequently Asked Questions

What is NOxyDERM used for?

NOxyDERM contains Benzalkonium Chloride. It is a liquid taken topical. Consult your doctor for specific uses.

Is NOxyDERM a controlled substance?

NOxyDERM is not classified as a controlled substance by the DEA.

What is the generic name for NOxyDERM?

The generic name for NOxyDERM is Benzalkonium Chloride. There are 12 other brand versions of Benzalkonium Chloride.

What is the NDC code for NOxyDERM .038 g/29.5mL?

The NDC (National Drug Code) for NOxyDERM .038 g/29.5mL is 83823-002, listed by NOxy Health Products.