Home NDC 70677-1088 Motion Sickness
Product NDC 70677-1088
11-digit product format 706771088
Labeler code 70677
Product ID 70677-1088_339f90ec-5d4a-433f-9324-7f7ffc37e22e
Type HUMAN OTC DRUG
Nonproprietary name Meclizine HCl
Dosage form TABLET
Route ORAL
Labeler Strategic Sourcing Services LLC
Application M009
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-04-06
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 70677-1088-1 Motion Sickness 8 in 1 BLISTER PACK TABLET 8 6 70677-1088-1 Motion Sickness 1 in 1 CARTON TABLET 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70677-1088 MOTION SICKNESS (MECLIZINE HCL) TABLET [STRATEGIC SOURCING SERVICES LLC] 5 Current NDC, 2 package rows 20240825_76fb6471-09b0-4c51-bacc-b3533b6aa971.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 Sample Exclude flag Status 70677-1088-1 70677108801 1 BLISTER PACK in 1 CARTON (70677-1088-1) / 8 TABLET in 1 BLISTER PACK 1 blister pack 2023-04-06 No No Current