Over-the-counter drug · OTC MONOGRAPH DRUG
Fuzion AB Foam (Benzalkonium chloride) NDC 66949-111
Benzalkonium chloride .13 g/100mL · Liquid · Topical · Zep Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 66949-111-16 | 6694901111666949011116 | 4800 mL in 1 CASE (66949-111-16)Marketed from Mar 10, 2017 |
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)
- Fuzion AB Foam
- Generic name (nonproprietary)
- benzalkonium chloride
- Active ingredients
- Benzalkonium chloride — .13 g/100mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- Zep Inc.NDC labeler code 66949
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 66949-111_46de4539-36b3-af75-e063-6294a90acfffSPL ID 46de4539-36b3-af75-e063-6294a90acfffSPL set ID b43ea64e-f7db-2250-e053-2995a90a43b3RxCUI 1046593UNII 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
N466949011116followed by a unit qualifier and the quantityPackage 66949-0111-16. 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 washing to decrease bacteria on hands.
Excerpt only. Read the full label for complete information.
About NDC 66949-111
- What is NDC 66949-111?
- 66949-111 is the product NDC for Fuzion AB Foam (benzalkonium chloride), Benzalkonium chloride .13 g/100mL liquid, listed with the FDA by Zep Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Fuzion AB Foam (Benzalkonium Chloride).
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- Zep Inc., NDC labeler code 66949. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Fuzion AB Foam?
- 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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