Motion Sickness Relief
- Product NDC
- 11673-356
- 11-digit product format
- 116730356
- Labeler code
- 11673
- Product ID
- 11673-356_3df6ca6b-8de9-4c46-e063-6294a90ab4e9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TARGET CORPORATION
- Application
- M009
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-11-05
- 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 |
|---|
| 11673-356-08 | Motion Sickness Relief | 1 in 1 CARTON | TABLET | 1 | | 2 |
| 11673-356-08 | Motion Sickness Relief | 8 in 1 BLISTER PACK | TABLET | 8 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 11673-356-08 | 11673035608 | 1 BLISTER PACK in 1 CARTON (11673-356-08) / 8 TABLET in 1 BLISTER PACK | 1 blister pack | 2025-11-05 | No | No | Current |