Drug
First Mark Ultra Foaming Antibacterial NDC Codes
First Mark Ultra Foaming Antibacterial is listed in the FDA NDC Directory as 1 finished product from 1 labeler.
Overview
Active ingredient: Benzalkonium chloride. Each product below links to its own NDC page with package NDCs in 10- and 11-digit form.
- Generic name
- Benzalkonium Chloride
- Active ingredients
- Benzalkonium chloride
- Labelers
- Performance Food Group
- Strengths
- Benzalkonium chloride 5 mg/mL
- Dosage forms
- Solution
- Routes
- Topical
- HCPCS / J-code
- None in Med-Code's directory for these products
- Package NDCs
- 1
NDC codes
Newest listings first. Each row links to the product’s NDC page.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) | HCPCS |
|---|---|---|---|---|---|---|
| First Mark Ultra Foaming Antibacterialbenzalkonium chloride | Benzalkonium chloride 5 mg/mL | SolutionTopical | Performance Food Group | 51042-001 | 51042-0001-10 | — |
First Mark Ultra Foaming Antibacterial: common questions
- What is the NDC for First Mark Ultra Foaming Antibacterial?
- First Mark Ultra Foaming Antibacterial has 1 product NDC, one for each strength, dosage form and labeler; each product NDC then has one package NDC per package size. Pick the row for your product above to see its package NDCs.
- Is there a J-code for First Mark Ultra Foaming Antibacterial?
- Med-Code's curated HCPCS directory has no drug-specific code for these products. Drugs dispensed by a pharmacy are billed by NDC. NDC vs J-code.
- Which NDC goes on a claim?
- The package NDC of what was given, in 11-digit form. How to convert a 10-digit NDC.