Home NDC 50844-338-22 Backache Relief
Product NDC 50844-338
Requested package NDC 50844-338-22
11-digit product format 508440338
Labeler code 50844
Product ID 50844-338_42236d39-cccf-47f2-af8c-ab7a2ea89076
Type HUMAN OTC DRUG
Nonproprietary name Magnesium Salicylate Tetrahydrate
Dosage form TABLET, FILM COATED
Route ORAL
Labeler L.N.K. International, Inc.
Application part343
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 1998-11-07
Marketing end 0000-00-00
Substance MAGNESIUM SALICYLATE
Active strength 580 mg/1
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded MAGNESIUM SALICYLATE ACTIVE INGREDIENT 41728CY7UX BACKACHE RELIEF EXTRA STRENGTH (MAGNESIUM SALICYLATE TETRAHYDRATE) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 4 SALICYLIC ACID ACTIVE MOIETY O414PZ4LPZ BACKACHE RELIEF EXTRA STRENGTH (MAGNESIUM SALICYLATE TETRAHYDRATE) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 4 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U BACKACHE RELIEF EXTRA STRENGTH (MAGNESIUM SALICYLATE TETRAHYDRATE) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 4 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO BACKACHE RELIEF EXTRA STRENGTH (MAGNESIUM SALICYLATE TETRAHYDRATE) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 4 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 BACKACHE RELIEF EXTRA STRENGTH (MAGNESIUM SALICYLATE TETRAHYDRATE) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 4 POLYDEXTROSE INACTIVE INGREDIENT VH2XOU12IE BACKACHE RELIEF EXTRA STRENGTH (MAGNESIUM SALICYLATE TETRAHYDRATE) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 4 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A BACKACHE RELIEF EXTRA STRENGTH (MAGNESIUM SALICYLATE TETRAHYDRATE) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 4 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP BACKACHE RELIEF EXTRA STRENGTH (MAGNESIUM SALICYLATE TETRAHYDRATE) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 4 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP BACKACHE RELIEF EXTRA STRENGTH (MAGNESIUM SALICYLATE TETRAHYDRATE) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 4 TRIACETIN INACTIVE INGREDIENT XHX3C3X673 BACKACHE RELIEF EXTRA STRENGTH (MAGNESIUM SALICYLATE TETRAHYDRATE) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 4
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 50844-338-22 50844033822 6 BLISTER PACK in 1 CARTON (50844-338-22) > 8 TABLET, FILM COATED in 1 BLISTER PACK 6 blister pack 1998-11-07 0000-00-00 No No Current