Motion Sickness Relief

Product NDC
59779-404
Requested package NDC
59779-404-21
11-digit product format
597790404
Labeler code
59779
Product ID
59779-404_cccec6fd-3619-4eb8-b255-659f8eac6d9d
Type
HUMAN OTC DRUG
Nonproprietary name
Meclizine HCl
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
CVS Pharmacy
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage59779-40459779-404-21DDiscontinued by firm2026-10-15

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59779-404MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET, CHEWABLE [CVS PHARMACY]13Legacy NDC20240421_a66e3d8a-5711-4c41-a424-14b8cdad5b68.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59779-404-21597790404212 BLISTER PACK in 1 CARTON (59779-404-21) > 8 TABLET, CHEWABLE in 1 BLISTER PACK2 blister pack2002-05-290000-00-00NoNoCurrent