Tinnitus Relief

Product NDC
43689-0009
Requested package NDC
43689-0009-1
11-digit product format
436890009
Labeler code
43689
Product ID
43689-0009_69a82b2e-dc1d-4690-9cd1-e4dc10c0f8ee
Type
HUMAN OTC DRUG
Nonproprietary name
Calcarea Carbonica, Chininum Sulphuricum, Kali Carbonicum, Lycopodium Clavatum, Salicylicum Acidum
Dosage form
TABLET
Route
ORAL
Labeler
The Magni Company
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2012-08-16
Marketing end
2023-01-18
Substance
LYCOPODIUM CLAVATUM SPORE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; POTASSIUM CARBONATE; QUININE SULFATE; SALICYLIC ACID
Active strength
6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes
Antimalarial [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage43689-000943689-0009-1DDiscontinued 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 · 15 matching rows.

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

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05DDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26DDiscontinued by firmf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31DDiscontinued by firm2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28DDiscontinued by firma1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21DDiscontinued by firmcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10DDiscontinued by firmcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31DDiscontinued by firm302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20DDiscontinued by firmed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10DDiscontinued by firm0efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08DDiscontinued by firmad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03DDiscontinued by firm367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09DDiscontinued by firm557ba5c1ecfa…9c80585c8c6e…
2021-12-27 23:28 UTC · source 2021-12-27IInactivated by FDA8dfbde2a14a4…c9ff85d89658…
2020-12-18 03:04 UTC · source 2020-12-17IInactivated by FDAe2bbac7714bc…27bdfed8d636…
2020-06-10 20:45 UTC · source 2020-06-10IInactivated by FDA9bebd1f3094a…5416666fcb17…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43689-0009-12022-02-03C16284748780-19d75b9d0-0163-f424-e053-dadaa90a57ceDRUG FACTS:
43689-0009-12020-01-31C16284748780-19d75b9d0-0163-f424-e053-dadaa90a57ceDRUG FACTS:

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y479TINNITUS RELIEF (CALCAREA CARBONICA, CHININUM SULPHURICUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SALICYLICUM ACIDUM) TABLET [THE MAGNI COMPANY]1
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE INGREDIENT2E32821G6ITINNITUS RELIEF (CALCAREA CARBONICA, CHININUM SULPHURICUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SALICYLICUM ACIDUM) TABLET [THE MAGNI COMPANY]1
POTASSIUM CARBONATEACTIVE INGREDIENTBQN1B9B9HATINNITUS RELIEF (CALCAREA CARBONICA, CHININUM SULPHURICUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SALICYLICUM ACIDUM) TABLET [THE MAGNI COMPANY]1
QUININE SULFATEACTIVE INGREDIENTKF7Z0E0Q2BTINNITUS RELIEF (CALCAREA CARBONICA, CHININUM SULPHURICUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SALICYLICUM ACIDUM) TABLET [THE MAGNI COMPANY]1
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZTINNITUS RELIEF (CALCAREA CARBONICA, CHININUM SULPHURICUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SALICYLICUM ACIDUM) TABLET [THE MAGNI COMPANY]1
CARBONATE IONACTIVE MOIETY7UJQ5OPE7DTINNITUS RELIEF (CALCAREA CARBONICA, CHININUM SULPHURICUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SALICYLICUM ACIDUM) TABLET [THE MAGNI COMPANY]1
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y479TINNITUS RELIEF (CALCAREA CARBONICA, CHININUM SULPHURICUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SALICYLICUM ACIDUM) TABLET [THE MAGNI COMPANY]1
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE MOIETY2E32821G6ITINNITUS RELIEF (CALCAREA CARBONICA, CHININUM SULPHURICUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SALICYLICUM ACIDUM) TABLET [THE MAGNI COMPANY]1
QUININEACTIVE MOIETYA7V27PHC7ATINNITUS RELIEF (CALCAREA CARBONICA, CHININUM SULPHURICUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SALICYLICUM ACIDUM) TABLET [THE MAGNI COMPANY]1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZTINNITUS RELIEF (CALCAREA CARBONICA, CHININUM SULPHURICUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SALICYLICUM ACIDUM) TABLET [THE MAGNI COMPANY]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UTINNITUS RELIEF (CALCAREA CARBONICA, CHININUM SULPHURICUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SALICYLICUM ACIDUM) TABLET [THE MAGNI COMPANY]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GTINNITUS RELIEF (CALCAREA CARBONICA, CHININUM SULPHURICUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SALICYLICUM ACIDUM) TABLET [THE MAGNI COMPANY]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30TINNITUS RELIEF (CALCAREA CARBONICA, CHININUM SULPHURICUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SALICYLICUM ACIDUM) TABLET [THE MAGNI COMPANY]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43689-0009-143689000901125 TABLET in 1 BOTTLE (43689-0009-1) 125 tablet2012-08-162023-01-18NoNoCurrent