Prescription drug · UNAPPROVED DRUG OTHER
Salicor (Triethanolamine salicylate) NDC 80425-0592
Tea-salicylate 40.2 mg/1 · Patch · Transdermal · Advanced Rx of Tennessee, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 80425-0592-1 | 80425059201 | 15 PATCH in 1 PACKAGE (80425-0592-1)Marketed from Aug 6, 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)
- Salicor
- Generic name (nonproprietary)
- triethanolamine salicylate
- Active ingredients
- Tea-salicylate — 40.2 mg/1
- Dosage form
- Patch
- Route
- Transdermal
- Labeler
- Advanced Rx of Tennessee, LLCNDC labeler code 80425
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Identifiers
- Product ID 80425-0592_5867340e-9221-2c40-e063-6294a90a2014SPL ID 5867340e-9221-2c40-e063-6294a90a2014SPL set ID 586733ff-065d-2eab-e063-6294a90a9485RxCUI 2722418, 2722423UNII H8O4040BHD
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. Transdermal products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N480425059201followed by a unit qualifier and the quantityPackage 80425-0592-01. 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
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATION AND USAGE Salicor™ is indicated for the temporary relief of minor aches and pains of muscles and joints associated with: arthritis, simple backache, muscle strains and sprains, bruises, bursitis, and dysmenorrhea. Salicor™ provides a localized analgesic effect directly at the site of pain, offering convenience and sustained relief compared to cream formulations.
Excerpt only. Read the full label for complete information.
About NDC 80425-0592
- What is NDC 80425-0592?
- 80425-0592 is the product NDC for Salicor (triethanolamine salicylate), Tea-salicylate 40.2 mg/1 patch, listed with the FDA by Advanced Rx of Tennessee, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Salicor (Triethanolamine salicylate).
- What is the active ingredient?
- Tea-salicylate.
- Who is the labeler?
- Advanced Rx of Tennessee, LLC, NDC labeler code 80425. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Salicor?
- 1 other product NDC are listed under this name. See all Salicor NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Salicor products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Salicortriethanolamine salicylate | Tea-salicylate 40.2 mg/1 | PatchTransdermal | Clinic Pharma | 83881-501 | 83881-0501-15 |