Salicor
- Product NDC
- 80425-0592
- Requested package NDC
- 80425-0592-1
- 11-digit product format
- 804250592
- Labeler code
- 80425
- Product ID
- 80425-0592_5867340e-9221-2c40-e063-6294a90a2014
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- triethanolamine salicylate
- Dosage form
- PATCH
- Route
- TRANSDERMAL
- Labeler
- Advanced Rx of Tennessee, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-08-06
- Substance
- TEA-SALICYLATE
- Active strength
- 40.2 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Salicor
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| TEA-SALICYLATE | 40.2 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| H8O4040BHD | Internal UNII lookup |
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 586733ff-065d-2eab-e063-6294a90a9485 | Available on FDA.report |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Salicor | TRIETHANOLAMINE SALICYLATE | Advanced Rx of Tennessee, LLC | 586733ff-065d-2eab-e063-6294a90a9485 | 2026-08-06 | Warnings | 80425-0592-1 80425-0592 80425059201 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 80425-0592-1 | 80425059201 | 15 PATCH in 1 PACKAGE (80425-0592-1) | 15 patch | 2026-08-06 | No | No | Current |