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Original Formula Motion Sickness Relief
Original Formula Motion Sickness Relief - 62011-0036-1 - (DIMENHYDRINATE)
Drug Information of Original Formula Motion Sickness Relief
| Product NDC: | 62011-0036 |
| Proprietary Name: | Original Formula Motion Sickness Relief |
| Non Proprietary Name: | DIMENHYDRINATE |
| Active Ingredient(s): | 50 mg/1 & nbsp; DIMENHYDRINATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Original Formula Motion Sickness Relief
| Product NDC: | 62011-0036 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120626 |
Package Information of Original Formula Motion Sickness Relief
| Package NDC: | 62011-0036-1 |
| Package Description: | 1 BLISTER PACK in 1 BOX (62011-0036-1) > 12 TABLET in 1 BLISTER PACK |
NDC Information of Original Formula Motion Sickness Relief
| NDC Code | 62011-0036-1 |
| Proprietary Name | Original Formula Motion Sickness Relief |
| Package Description | 1 BLISTER PACK in 1 BOX (62011-0036-1) > 12 TABLET in 1 BLISTER PACK |
| Product NDC | 62011-0036 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIMENHYDRINATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120626 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | DIMENHYDRINATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
