Over-the-counter drug · OTC MONOGRAPH DRUG
Dynarex Povidone Iodine Prep Solution (Povidone iodine prep solution) NDC 67777-141
Povidone-iodine 10 mg/mL · Liquid · Topical · Dynarex Corporation
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 67777-141-31 | 6777701413167777014131 | 48 BOTTLE in 1 CASE (67777-141-31) / 118 mL in 1 BOTTLE (67777-141-30)Marketed from May 8, 2018 | |
| 67777-141-41 | 6777701414167777014141 | 24 BOTTLE in 1 CASE (67777-141-41) / 237 mL in 1 BOTTLE (67777-141-40)Marketed from May 8, 2018 | |
| 67777-141-51 | 6777701415167777014151 | 24 BOTTLE in 1 CASE (67777-141-51) / 473 mL in 1 BOTTLE (67777-141-50)Marketed from May 8, 2018 | |
| 67777-141-61 | 6777701416167777014161 | 4 BOTTLE in 1 CASE (67777-141-61) / 3790 mL in 1 BOTTLE (67777-141-60)Marketed from May 8, 2018 |
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)
- Dynarex Povidone Iodine Prep Solution
- Generic name (nonproprietary)
- povidone iodine prep solution
- Active ingredients
- Povidone-iodine — 10 mg/mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- Dynarex CorporationNDC labeler code 67777
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 003
- Marketing start
- Listing expires
- Identifiers
- Product ID 67777-141_275871a0-3173-c7fa-e063-6394a90ac014SPL ID 275871a0-3173-c7fa-e063-6394a90ac014SPL set ID 6bb4d55b-2be7-3549-e053-2a91aa0a2bb0RxCUI 312564UNII 85H0HZU99MUPC 0616784141329
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
N467777014131followed by a unit qualifier and the quantityPackage 67777-0141-31. 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)
Use For preparation of the skin prior to surgery. Helps reduce bacteria that potentially can cause skin infection
Excerpt only. Read the full label for complete information.
About NDC 67777-141
- What is NDC 67777-141?
- 67777-141 is the product NDC for Dynarex Povidone Iodine Prep Solution, Povidone-iodine 10 mg/mL liquid, listed with the FDA by Dynarex Corporation. It has 4 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Dynarex Povidone Iodine Prep Solution (Povidone Iodine Prep Solution).
- What is the active ingredient?
- Povidone-iodine.
- Who is the labeler?
- Dynarex Corporation, NDC labeler code 67777. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Dynarex Povidone Iodine Prep Solution?
- 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 M 003
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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