Motion Sickness Relief
- Product NDC
- 30142-943
- 11-digit product format
- 301420943
- Labeler code
- 30142
- Product ID
- 30142-943_0960100c-9b4b-40da-9ecd-2791724d3a53
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Meclizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- M009
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-06-03
- 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 |
|---|
| 30142-943-19 | Motion Sickness Relief | 8 in 1 BOTTLE, PLASTIC | TABLET | 8 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 30142-943 | MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET [KROGER COMPANY] | 10 | Current NDC, Legacy NDC, 1 package rows | 20241105_64e0496c-5e09-46e9-94b9-624163d71b60.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 |
|---|
| 30142-943-19 | 30142094319 | 8 TABLET in 1 BOTTLE, PLASTIC (30142-943-19) | 8 tablet | 2019-06-03 | 0000-00-00 | No | No | Current |