Home NDC 47682-074-99 Medique Back Pain Relief
Product NDC 47682-074
Requested package NDC 47682-074-99
11-digit product format 476820074
Labeler code 47682
Product ID 47682-074_3e4cc387-246f-c235-e063-6294a90aaa86
Type HUMAN OTC DRUG
Nonproprietary name Magnesium Salicylate Tetrahydrate
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Unifirst First Aid Corporation
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-09-26
Substance MAGNESIUM SALICYLATE
Active strength 580 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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…
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 Medique Back Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM SALICYLATE 580 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 41728CY7UX Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198742 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 47682-074-36 Medique Back Pain Relief 75 in 1 BOX TABLET, FILM COATED 75 5 47682-074-36 Medique Back Pain Relief 2 in 1 PACKET TABLET, FILM COATED 2 5 47682-074-80 Medique Back Pain Relief 40 in 1 BOX TABLET, FILM COATED 40 5 47682-074-99 Medique Back Pain Relief 2 in 1 PACKET TABLET, FILM COATED 2 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 47682-074 MEDIQUE BACK PAIN RELIEF (MAGNESIUM SALICYLATE TETRAHYDRATE) TABLET, FILM COATED [UNIFIRST FIRST AID CORPORATION] 4 Current NDC, Legacy NDC, 4 package rows 20240915_e5563a0a-776a-83d4-e053-2a95a90a9500.zip
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 39 of 79 · 1,576 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 47682-074-99 47682007499 2 TABLET, FILM COATED in 1 PACKET (47682-074-99) 2022-09-26 No No Current