Home NDC 69842-395 Motion Sickness Relief
Product NDC 69842-395
11-digit product format 698420395
Labeler code 69842
Product ID 69842-395_05742d9a-1a56-4982-b872-366f86091bbb
Type HUMAN OTC DRUG
Nonproprietary name Meclizine HCl
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler CVS PHARMACY, INC.
Application part336
Marketing category OTC MONOGRAPH FINAL
Marketing start 2017-11-28
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 995632 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 69842-395-54 Motion Sickness Relief 2 in 1 POUCH TABLET, CHEWABLE 2 1 69842-395-54 Motion Sickness Relief 15 in 1 CARTON TABLET, CHEWABLE 15 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-395 MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET, CHEWABLE [CVS PHARMACY, INC.] 1 Current NDC, Legacy NDC, 2 package rows 20171129_eb137393-889c-4498-95cd-6c0e6e126c5f.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 1 · 1 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 69842-395-54 69842039554 15 POUCH in 1 CARTON (69842-395-54) / 2 TABLET, CHEWABLE in 1 POUCH 15 pouch 2017-11-28 0000-00-00 No No Current