Pain Aid BRF

Product NDC
35418-801
11-digit product format
354180801
Labeler code
35418
Product ID
35418-801_19c6267c-4718-4a75-8336-edaac16088c5
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen Magnesium Salicylate
Dosage form
TABLET
Route
ORAL
Labeler
Zee Medical Inc
Application
part343
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2012-08-19
Marketing end
0000-00-00
Substance
MAGNESIUM SALICYLATE; ACETAMINOPHEN
Active strength
250 mg/1; mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct35418-801DDiscontinued by firm2026-10-05
excluded packagepackage35418-80135418-801-68DDiscontinued by firm2026-10-05

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 · 24 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage35418-801-68d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage35418-801-68f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage35418-801-682ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage35418-801-68a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage35418-801-68cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage35418-801-68cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage35418-801-68302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage35418-801-68ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage35418-801-680efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage35418-801-68ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage35418-801-68367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage35418-801-68557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACETAMINOPHENACTIVE INGREDIENT362O9ITL9DPAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1
MAGNESIUM SALICYLATEACTIVE INGREDIENT41728CY7UXPAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1
ACETAMINOPHENACTIVE MOIETY362O9ITL9DPAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZPAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UPAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1
D&C YELLOW NO. 10INACTIVE INGREDIENT35SW5USQ3GPAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1
FD&C YELLOW NO. 6INACTIVE INGREDIENTH77VEI93A8PAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1
POLYDEXTROSEINACTIVE INGREDIENTVH2XOU12IEPAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1
POLYETHYLENE GLYCOL 300INACTIVE INGREDIENT5655G9Y8AQPAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1
POVIDONEINACTIVE INGREDIENTFZ989GH94EPAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4PAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJPAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APPAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPPAIN AID BRF (ACETAMINOPHEN MAGNESIUM SALICYLATE) TABLET [ZEE MEDICAL INC]1