Motion Sickness Relief
- Product NDC
- 0363-1980
- 11-digit product format
- 003631980
- Labeler code
- 0363
- Product ID
- 0363-1980_2a9eed24-8e70-4f4f-9a42-56380d850fa8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dimenhydrinate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Walgreen Company
- Application
- M009
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-10-22
- 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 |
|---|---|
| ace7eba4-e033-48f5-8533-c3ea9dfc32b0 | 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 |
|---|---|---|---|---|---|---|
| 0363-1980-08 | Motion Sickness Relief | 6 in 1 BLISTER PACK | TABLET | 6 | 6 | |
| 0363-1980-08 | Motion Sickness Relief | 4 in 1 CARTON | TABLET | 4 | 6 |
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 |
|---|---|---|---|---|---|---|
| Airmit Ace | DIMENHYDRINATE | Sato Pharmaceutical Co., Ltd. | a98d252d-4cfa-496a-ab2c-627f45f0d7d9 | 2023-12-01 | Warnings | M009 |
| Meclizine HCl | MECLIZINE HYDROCHLORIDE | BluePoint Laboratories | d9cae5a6-8d4b-bdaf-e053-2995a90a7d44 | 2023-11-17 | Warnings | M009 |
| ZenTrip Motion Sickness | MECLIZINE HYDROCHLORIDE | Sato Pharmaceutical Co., LTD | bd86c4c7-b6f0-e3e8-e053-2995a90a4454 | 2023-11-03 | Warnings | M009 |
| Travel-Ease | MECLIZINE HCL | Geri-Care Pharmaceutical Corp | e3c64eb9-4972-29d9-e053-2a95a90a2a8a | 2023-10-25 | Warnings | M009 |
| Gravol | DIMENHYDRINATE | Church & Dwight Co., Inc. | d95240bb-02f2-3226-e053-2995a90afacd | 2022-03-03 | Warnings | M009 |
| Allergy DyeFree | ALLERGY DYEFREE | Allegiant Health | 15736bb8-5a5b-489d-83ad-4cf34ec62956 | 2021-04-26 | Warnings | M009 |
| Motion Sickness Relief | DIMENHYDRINATE 50MG | Allegiant Health | 7b0aa993-f08f-4dff-a82d-f35b3ebe3cc1 | 2019-12-12 | Warnings | M009 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 198603 | dimenhyDRINATE 50 MG Oral Tablet | PSN | ace7eba4-e033-48f5-8533-c3ea9dfc32b0 | 6 |
| 198603 | dimenhydrinate 50 MG Oral Tablet | SCD | ace7eba4-e033-48f5-8533-c3ea9dfc32b0 | 6 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0363-1980-08 | 00363198008 | 4 BLISTER PACK in 1 CARTON (0363-1980-08) / 6 TABLET in 1 BLISTER PACK | 4 blister pack | 2021-10-22 | 0000-00-00 | No | No | Current |