Home NDC 83881-501 Salicor
Product NDC 83881-501
11-digit product format 838810501
Labeler code 83881
Product ID 83881-501_41b01e12-6a3b-b34c-e063-6394a90a98e3
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 2026-12-31
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 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TEA-SALICYLATE 40.2 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H8O4040BHD Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2722418 Internal RxNorm lookup 2722423 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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
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.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Status 83881-501-15 83881050115 15 in 1 PACKAGE Historical