Drugplain

FIRST MARK ULTRA FOAMING ANTIBACTERIAL 5 mg/mL

Benzalkonium Chloride · SOLUTION · Performance Food Group

No Recall History
Plain English

FIRST MARK ULTRA FOAMING ANTIBACTERIAL is a solution containing benzalkonium chloride at 5 mg/mL, taken topical. Manufactured by Performance Food Group.

Key Facts

Brand Name
FIRST MARK ULTRA FOAMING ANTIBACTERIAL
Generic Name
Benzalkonium Chloride
NDC Code (Product)
51042-001
Manufacturer
Performance Food Group
Strength
5 mg/mL
Dosage Form
SOLUTION
Route
TOPICAL
Marketing Status
Application #
505G(a)(3)
Marketing Start
08/12/2015

Recall History

No Recall History

Frequently Asked Questions

What is FIRST MARK ULTRA FOAMING ANTIBACTERIAL used for?

FIRST MARK ULTRA FOAMING ANTIBACTERIAL contains Benzalkonium Chloride. It is a solution taken topical. Consult your doctor for specific uses.

Is FIRST MARK ULTRA FOAMING ANTIBACTERIAL a controlled substance?

FIRST MARK ULTRA FOAMING ANTIBACTERIAL is not classified as a controlled substance by the DEA.

What is the generic name for FIRST MARK ULTRA FOAMING ANTIBACTERIAL?

The generic name for FIRST MARK ULTRA FOAMING ANTIBACTERIAL is Benzalkonium Chloride. There are 12 other brand versions of Benzalkonium Chloride.

What is the NDC code for FIRST MARK ULTRA FOAMING ANTIBACTERIAL 5 mg/mL?

The NDC (National Drug Code) for FIRST MARK ULTRA FOAMING ANTIBACTERIAL 5 mg/mL is 51042-001, listed by Performance Food Group.