Over-the-counter drug · OTC MONOGRAPH DRUG
First Mark Ultra Foaming Antibacterial (Benzalkonium chloride) NDC 51042-001
Benzalkonium chloride 5 mg/mL · Solution · Topical · Performance Food Group
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 51042-001-10 | 5104200011051042000110 | 1250 mL in 1 BOTTLE (51042-001-10)Marketed from Nov 29, 2021 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- First Mark Ultra Foaming Antibacterial
- Generic name (nonproprietary)
- benzalkonium chloride
- Active ingredients
- Benzalkonium chloride — 5 mg/mL
- Dosage form
- Solution
- Route
- Topical
- Labeler
- Performance Food GroupNDC labeler code 51042
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 51042-001_f855444d-b8b3-4200-8ebe-481bb30ee25fSPL ID f855444d-b8b3-4200-8ebe-481bb30ee25fSPL set ID 968c0f18-d0b6-4f29-b001-00ac314a3bddUNII F5UM2KM3W7
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N451042000110followed by a unit qualifier and the quantityPackage 51042-0001-10. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses For handwashing to decrease bacteria on the skin
Excerpt only. Read the full label for complete information.
About NDC 51042-001
- What is NDC 51042-001?
- 51042-001 is the product NDC for First Mark Ultra Foaming Antibacterial, Benzalkonium chloride 5 mg/mL solution, listed with the FDA by Performance Food Group. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- First Mark Ultra Foaming Antibacterial (Benzalkonium Chloride).
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- Performance Food Group, NDC labeler code 51042. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for First Mark Ultra Foaming Antibacterial?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Other NDCs under 505G(a)(3)
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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