Home NDC 50804-214-03 Arthritis Relief
Product NDC 50804-214
Requested package NDC 50804-214-03
11-digit product format 508040214
Labeler code 50804
Product ID 50804-214_aca0a812-b11a-0a0e-e053-2995a90adb4b
Type HUMAN OTC DRUG
Nonproprietary name Trolamin Salicylate 10%
Dosage form CREAM
Route TOPICAL
Labeler Geiss, Destin & Dunn, Inc
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2014-06-27
Marketing end 0000-00-00
Substance TROLAMINE SALICYLATE
Active strength 10 g/100g
NDC exclude flag No
Listing certified through 2021-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 50804-214 50804-214-03 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
FDA-Initiated Inactive NDC Indexing# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50804-214 ARTHRITIS RELIEF MAXIMUM STRENGTH (TROLAMIN SALICYLATE 10%) CREAM [GEISS, DESTIN & DUNN, INC] 2 Legacy NDC 20240118_aca0a812-b119-0a0e-e053-2995a90adb4b.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 50804-214-03 50804021403 1 TUBE in 1 CARTON (50804-214-03) > 85 g in 1 TUBE 1 tube 2014-06-27 0000-00-00 No No Current