Salicor
- Product NDC
- 83881-501
- 11-digit product format
- 838810501
- Labeler code
- 83881
- Product ID
- 83881-501_5c3f6b9a-3151-7f93-e063-6394a90a4e43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- triethanolamine salicylate
- Dosage form
- PATCH
- Route
- TRANSDERMAL
- Labeler
- Clinic Pharma
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-10-22
- 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 table| Ingredient | Strength |
|---|
| TEA-SALICYLATE | 40.2 mg/1 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83881-501-15 | Salicor | 15 in 1 PACKAGE | PATCH | 15 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83881-501-15 | 83881050115 | 15 PATCH in 1 PACKAGE (83881-501-15) | 15 patch | 2026-05-01 | No | No | Current |