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Multi- Symptom Relief DayTime
Multi- Symptom Relief DayTime - 59726-470-08 - (ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCL)
Drug Information of Multi- Symptom Relief DayTime
| Product NDC: | 59726-470 |
| Proprietary Name: | Multi- Symptom Relief DayTime |
| Non Proprietary Name: | ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCL |
| Active Ingredient(s): | 325; 10; 5 mg/1; mg/1; mg/1 & nbsp; ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Multi- Symptom Relief DayTime
| Product NDC: | 59726-470 |
| Labeler Name: | P and L Development of New York Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120201 |
Package Information of Multi- Symptom Relief DayTime
| Package NDC: | 59726-470-08 |
| Package Description: | 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (59726-470-08) |
NDC Information of Multi- Symptom Relief DayTime
| NDC Code | 59726-470-08 |
| Proprietary Name | Multi- Symptom Relief DayTime |
| Package Description | 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (59726-470-08) |
| Product NDC | 59726-470 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCL |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20120201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | P and L Development of New York Corporation |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
