Motion Sickness Relief
- Product NDC
- 46122-535
- 11-digit product format
- 461220535
- Labeler code
- 46122
- Product ID
- 46122-535_47d10e3c-8ec0-4776-980e-ded451592a23
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Meclizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Amerisource Bergen
- Application
- M009
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2002-06-24
- 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 Relief
- 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 |
|---|
| 46122-535-51 | Motion Sickness Relief | 1 in 1 CARTON | TABLET | 1 | | 10 |
| 46122-535-51 | Motion Sickness Relief | 8 in 1 BLISTER PACK | TABLET | 8 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 46122-535 | MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET [AMERISOURCE BERGEN] | 9 | Current NDC, Legacy NDC, 2 package rows | 20241113_503f62e7-8ec8-4409-9697-4efef4ff7b15.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 |
|---|
| 46122-535-51 | 46122053551 | 1 BLISTER PACK in 1 CARTON (46122-535-51) / 8 TABLET in 1 BLISTER PACK | 1 blister pack | 2002-06-24 | 0000-00-00 | No | No | Current |