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Cold Relief Daytime Multi-Symptom
Cold Relief Daytime Multi-Symptom - 59779-560-07 - (Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr)
Drug Information of Cold Relief Daytime Multi-Symptom
| Product NDC: | 59779-560 |
| Proprietary Name: | Cold Relief Daytime Multi-Symptom |
| Non Proprietary Name: | Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr |
| Active Ingredient(s): | 325; 10; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cold Relief Daytime Multi-Symptom
| Product NDC: | 59779-560 |
| Labeler Name: | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080329 |
Package Information of Cold Relief Daytime Multi-Symptom
| Package NDC: | 59779-560-07 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (59779-560-07) > 36 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Information of Cold Relief Daytime Multi-Symptom
| NDC Code | 59779-560-07 |
| Proprietary Name | Cold Relief Daytime Multi-Symptom |
| Package Description | 1 BLISTER PACK in 1 CARTON (59779-560-07) > 36 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 59779-560 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20080329 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
