Home NDC 46122-535 Motion Sickness Relief
Product NDC 46122-535
11-digit product format 461220535
Labeler code 46122
Product ID 46122-535_47d10e3c-8ec0-4776-980e-ded451592a23
Type HUMAN OTC DRUG
Nonproprietary name Meclizine HCl
Dosage form TABLET
Route ORAL
Labeler Amerisource Bergen
Application M009
Marketing category OTC MONOGRAPH DRUG
Marketing start 2002-06-24
Substance MECLIZINE HYDROCHLORIDE
Active strength 25 mg/1
Pharmacologic classes Antiemetic [EPC], Emesis Suppression [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 Motion Sickness Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MECLIZINE HYDROCHLORIDE 25 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination HDP7W44CIO Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 995666 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 46122-535-51 Motion Sickness Relief 1 in 1 CARTON TABLET 1 10 46122-535-51 Motion Sickness Relief 8 in 1 BLISTER PACK TABLET 8 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 46122-535 MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET [AMERISOURCE BERGEN] 9 Current NDC, Legacy NDC, 2 package rows 20241113_503f62e7-8ec8-4409-9697-4efef4ff7b15.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 6 of 6 · 107 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 46122-535-51 46122053551 1 BLISTER PACK in 1 CARTON (46122-535-51) / 8 TABLET in 1 BLISTER PACK 1 blister pack 2002-06-24 0000-00-00 No No Current