Motion Sickness Relief
- Product NDC
- 50844-199
- 11-digit product format
- 508440199
- Labeler code
- 50844
- Product ID
- 50844-199_6a8965ee-3d03-48bd-9271-6ca40246f42e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dimenhydrinate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- L.N.K. International, Inc.
- 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
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
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| DIMENHYDRINATE | 50 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| JB937PER5C | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 198603 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 95aae32f-6b3f-469d-86a5-c201a53f862a | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 0e2e0f88-b076-afe1-4bdd-32bca4375bec | Product name | 3 | 20250127 |
| 3e48c9c4-918d-5d23-2f0b-d2398b06be54 | Product name | 1 | 20140508 |
| 865c72dd-0d94-daac-f728-ddd4ded2a79e | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50844-199-02 | Motion Sickness Relief | 2 in 1 CARTON | TABLET | 2 | 11 | |
| 50844-199-02 | Motion Sickness Relief | 6 in 1 BLISTER PACK | TABLET | 6 | 11 |
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Dimenhydrinate | DIMENHYDRINATE | LEADER/ Cardinal Health 110, Inc. | 7c4adbdb-9bce-0c9c-e053-2a91aa0a8107 | 2026-02-20 | Warnings | M009 |
| Dramamine Less Drowsy | MECLIZINE HYDROCHLORIDE | Navajo Manufacturing Company Inc. | 4b203479-ba8d-7237-e063-6294a90ae6cb | 2026-02-18 | Warnings | M009 |
| Meclizine Hydrochloride | MECLIZINE HYDROCHLORIDE | NuCare Pharmaceuticals,Inc. | d0d8b376-8fe9-8776-e053-2a95a90ae651 | 2026-01-27 | Warnings | M009 |
| Motion Sickness Relief | MECLIZINE HCL | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 4f806804-48c7-414e-a177-5d3daf5b22e3 | 2026-01-20 | Warnings | M009 |
| MECLIZINE | MECLIZINE HCL 25 MG | Bi-Mart | 2e2c8189-c026-48f8-bbc6-371498ccf444 | 2026-01-13 | Warnings | M009 |
| Motion Sickness Relief | MECLIZINE HCL | United Natural Foods, Inc. dba UNFI | 108bb943-529f-4510-b770-b54eca493ae0 | 2026-01-12 | Warnings | M009 |
| Less Drowsy Motion Sickness Relief | MECLIZINE HCL | Rite Aid Corporation | 2f9ebe6b-ffde-41de-9eaa-b03d87d33005 | 2026-01-09 | Warnings | M009 |
| Motion Sickness Relief | DIMENHYDRINATE | Rite Aid Corporation | 4f532984-aeee-4dde-972c-742bdf12868f | 2026-01-07 | Warnings | M009 |
| Motion Sickness Relief | MECLIZINE HCL | Family Dollar Services Inc | e34126e3-52ef-4999-bf61-cba9b1818259 | 2026-01-05 | Warnings | M009 |
| CVS Motion Sickness Fast Melting | MECLIZINE HYDROCHLORIDE | CVS Pharmacy, Inc. | 2a723bce-a581-4558-b028-22f1f9125dd5 | 2025-12-30 | Warnings | M009 |
| Wal-Dram 2 Quick-Dissolving | MECLIZINE HYDROCHLORIDE | Walgreen Co. | f3116203-1b8f-438a-b779-7bdd90eaf79e | 2025-12-30 | Warnings | M009 |
| MECLIZINE | MECLIZINE HCL 12.5 MG | Pharbest Pharmaceuticals, Inc. | 8b3c9283-b618-4d57-9f15-7cf73e8737f5 | 2025-12-24 | Warnings | M009 |
| MECLIZINE | MECLIZINE HCL 25MG | Pharbest Pharmaceuticals, Inc. | 4bac2765-045c-405e-8006-8c5cfdfa89bc | 2025-12-24 | Warnings | M009 |
| DRAMAMINE | MECLIZINE HYDROCHLORIDE | Medtech Products Inc. | fdcbcc4e-9370-4975-8905-1f12c73fdc8c | 2025-12-23 | Warnings | M009 |
| DRAMAMINE | MECLIZINE HYDROCHLORIDE | Medtech Products Inc. | 3a960d43-62aa-464e-92b9-d83042ba02bf | 2025-12-23 | Warnings | M009 |
| DRAMAMINE | MECLIZINE HYDROCHLORIDE | Medtech Products Inc. | 6efd3473-ee14-4ee0-8a58-d15a64a9224a | 2025-12-18 | Warnings | M009 |
| Motion Sickness Relief | MECLIZINE HCL | Rite Aid Corporation | e599dc64-ac10-4f4e-9318-e9fab0526488 | 2025-11-15 | Warnings | M009 |
| Motion Sickness Relief | MECLIZINE HCL | Kroger Company | 64e0496c-5e09-46e9-94b9-624163d71b60 | 2025-11-05 | Warnings | M009 |
| Motion Sickness Relief | MECLIZINE HCL | Walgreen Company | 27bd9c74-c85e-4eeb-9e43-4120f9001187 | 2025-11-05 | Warnings | M009 |
| Dramamine Original Formula | DIMENHYDRINATE | Medtech Products Inc. | f9302a5a-295a-4501-9332-e3f5eb387362 | 2025-10-23 | Warnings | M009 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 198603 | dimenhyDRINATE 50 MG Oral Tablet | PSN | 95aae32f-6b3f-469d-86a5-c201a53f862a | 11 |
| 198603 | dimenhydrinate 50 MG Oral Tablet | SCD | 95aae32f-6b3f-469d-86a5-c201a53f862a | 11 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50844-199-02 | 50844019902 | 2 BLISTER PACK in 1 CARTON (50844-199-02) / 6 TABLET in 1 BLISTER PACK | 2 blister pack | 1992-12-01 | 0000-00-00 | No | No | Current |