Over-the-counter drug · OTC MONOGRAPH DRUG
Zoviro (Alcohol) NDC 83814-005
Alcohol 70 mL/100mL · Liquid · Topical · Zoviro, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 83814-005-01 | 8381400050183814000501 | 60 mL in 1 BOTTLE (83814-005-01)Marketed from Jan 9, 2024 |
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)
- Zoviro
- Generic name (nonproprietary)
- alcohol
- Active ingredients
- Alcohol — 70 mL/100mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- Zoviro, LLCNDC labeler code 83814
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 83814-005_5bf5e00c-bee3-ed72-e063-6394a90ae745SPL ID 5bf5e00c-bee3-ed72-e063-6394a90ae745
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
N483814000501followed by a unit qualifier and the quantityPackage 83814-0005-01. 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
The FDA listing for this product does not reference a label (SPL) set.
About NDC 83814-005
- What is NDC 83814-005?
- 83814-005 is the product NDC for Zoviro (alcohol), Alcohol 70 mL/100mL liquid, listed with the FDA by Zoviro, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Zoviro (Alcohol).
- What is the active ingredient?
- Alcohol.
- Who is the labeler?
- Zoviro, LLC, NDC labeler code 83814. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Zoviro?
- 5 other product NDCs are listed under this name. See all Zoviro NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Zoviro products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Zoviroalcohol | Alcohol 70 mL/100mL | GelTopical | Zoviro, LLC | 83814-007 | 83814-0007-01 |
| Zovirobenzalkonium chloride | Benzalkonium chloride .12 g/100mL | LiquidTopical | Zoviro, LLC | 83814-006 | 83814-0006-01 |
| Zovirobenzalkonium chloride | Benzalkonium chloride .13 g/100g | SwabTopical | Zoviro, LLC | 83814-004 | 83814-0004-01 |
| Zovirobenzalkonium chloride | Benzalkonium chloride .13 g/100g | SwabTopical | Zoviro, LLC | 83814-001 | 83814-0001-01 |
| Zovirobenzalkonium chloride | Benzalkonium chloride .13 g/100g | SwabTopical | Zoviro, LLC | 83814-003 | 83814-0003-01 |
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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