Home NDC 59779-198-07 Motion Sickness
Product NDC 59779-198
Requested package NDC 59779-198-07
11-digit product format 597790198
Labeler code 59779
Product ID 59779-198_e72c2541-7d9f-435a-8ca7-c9d9fa116ea3
Type HUMAN OTC DRUG
Nonproprietary name Dimenhydrinate
Dosage form TABLET
Route ORAL
Labeler CVS Pharmacy
Application M009
Marketing category OTC MONOGRAPH DRUG
Marketing start 1992-12-01
Substance DIMENHYDRINATE
Active strength 50 mg/1
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 DIMENHYDRINATE 50 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination JB937PER5C Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198603 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DIMENHYDRINATE ACTIVE INGREDIENT JB937PER5C MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 7 DIPHENHYDRAMINE ACTIVE MOIETY 8GTS82S83M MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 7 CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS INACTIVE INGREDIENT L11K75P92J MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 7 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 7 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 7 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 7 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 7
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 59779-198-07 59779019807 6 BLISTER PACK in 1 CARTON (59779-198-07) / 6 TABLET in 1 BLISTER PACK 6 blister pack 1992-12-01 0000-00-00 No No Current