Home NDC 37808-903-12 Motion Sickness
Product NDC 37808-903
Requested package NDC 37808-903-12
11-digit product format 378080903
Labeler code 37808
Product ID 37808-903_b8856f56-be6c-4f40-833f-e8866786ab82
Type HUMAN OTC DRUG
Nonproprietary name Meclizine HCl
Dosage form TABLET
Route ORAL
Labeler H E B
Application M009
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-06-24
Substance MECLIZINE HYDROCHLORIDE
Active strength 25 mg/1
Pharmacologic classes Antiemetic [EPC], Emesis Suppression [PE]
NDC exclude flag No
Listing certified through 2027-12-31
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
Listing expiration 2027-12-31 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 37808-903-12 Motion Sickness 100 in 1 BOTTLE TABLET 100 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-903 MOTION SICKNESS (MECLIZINE HCL) TABLET [H E B] 8 Current NDC, Legacy NDC, 1 package rows 20240825_9837e9af-c542-4c0f-be33-94927d67c6a7.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 1 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 37808-903-12 37808090312 100 TABLET in 1 BOTTLE (37808-903-12) 100 tablet 2019-06-24 0000-00-00 No No Current