Motion Sickness
- Product NDC
- 37808-903
- 11-digit product format
- 378080903
- Labeler code
- 37808
- Product ID
- 37808-903_3473b0b6-6443-4b2d-b8b1-89350fc754ad
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Meclizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- H E B
- Application
- M009
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-06-24
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Motion Sickness
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MECLIZINE HYDROCHLORIDE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | HDP7W44CIO |
| Rxcui | 995666 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37808-903-12 | Motion Sickness | 100 in 1 BOTTLE | TABLET | 100 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-903 | MOTION SICKNESS (MECLIZINE HCL) TABLET [H E B] | 8 | Current NDC, Legacy NDC, 1 package rows | 20240825_9837e9af-c542-4c0f-be33-94927d67c6a7.zip |
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 |
|---|
| 37808-903-12 | 37808090312 | 100 TABLET in 1 BOTTLE (37808-903-12) | 100 tablet | 2019-06-24 | 0000-00-00 | No | No | Current |