FDA.reportPublic FDA data

Motion Sickness Relief

Product NDC
11822-0404
11-digit product format
118220404
Labeler code
11822
Product ID
11822-0404_428186b7-e452-425b-a8f7-e33f8db82379
Type
HUMAN OTC DRUG
Nonproprietary name
Meclizine HCl
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
Rite Aid Corporation
Application
part336
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2002-05-29
Marketing end
0000-00-00
Substance
MECLIZINE HYDROCHLORIDE
Active strength
25 mg/1
Pharmacologic classes
Antiemetic [EPC], Emesis Suppression [PE]
NDC exclude flag
No
Listing certified through
2023-12-31
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 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct11822-0404DDiscontinued by firm2026-08-10
excluded packagepackage11822-040411822-0404-2DDiscontinued by firm2026-08-10
excluded packagepackage11822-040411822-0404-4DDiscontinued by firm2026-08-10

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 dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MECLIZINE HYDROCHLORIDEACTIVE INGREDIENTHDP7W44CIOMOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET, CHEWABLE [RITE AID]7
MECLIZINEACTIVE MOIETY3L5TQ84570MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET, CHEWABLE [RITE AID]7
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOAMOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET, CHEWABLE [RITE AID]7
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET, CHEWABLE [RITE AID]7
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJMOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET, CHEWABLE [RITE AID]7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-0404MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET, CHEWABLE [RITE AID CORPORATION]18Legacy NDC20240921_1d2f5ae4-8a0a-455e-87d1-61d7d07d3455.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-0404-2118220404022 BLISTER PACK in 1 CARTON (11822-0404-2) > 8 TABLET, CHEWABLE in 1 BLISTER PACK2 blister pack2002-05-290000-00-00NoNoCurrent
11822-0404-4118220404041 BLISTER PACK in 1 CARTON (11822-0404-4) > 2 TABLET, CHEWABLE in 1 BLISTER PACK1 blister pack2002-05-290000-00-00NoNoCurrent