Over-the-counter drug · ANDA
Docosanol NDC 51672-1406
Docosanol 100 mg/g · Cream · Topical · Sun Pharmaceutical Industries, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 51672-1406-2 | 51672140602 | 2 TUBE in 1 PACKAGE (51672-1406-2) / 2 g in 1 TUBEMarketed from Oct 26, 2023 | |
| 51672-1406-3 | 51672140603 | 1 TUBE in 1 PACKAGE (51672-1406-3) / 2 g in 1 TUBEMarketed from Oct 26, 2023 | |
| 51672-1406-5 | 51672140605 | 1 TUBE in 1 CARTON (51672-1406-5) / 2 g in 1 TUBEMarketed from Sep 1, 2026 | |
| 51672-1406-6 | 51672140606 | 2 TUBE in 1 CARTON (51672-1406-6) / 2 g in 1 TUBEMarketed from Sep 1, 2026 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
- Docosanol
- Generic name (nonproprietary)
- docosanol
- Active ingredients
- Docosanol — 100 mg/g
- Dosage form
- Cream
- Route
- Topical
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 214454
- Marketing start
- Listing expires
- Identifiers
- Product ID 51672-1406_57993b31-36bc-4768-e063-6294a90a9ee0SPL ID 57993b31-36bc-4768-e063-6294a90a9ee0SPL set ID 5079b009-7f34-4d34-8f01-821365f04ca2RxCUI 797534UNII 9G1OE216XYUPC 0351672140656, 0351672140632
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
N451672140602followed by a unit qualifier and the quantityPackage 51672-1406-02. 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 treats cold sores/fever blisters on the face or lips shortens healing time and duration of symptoms: tingling, pain, burning, and/or itching
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 214454
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.