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DayRelief
DayRelief - 55312-656-30 - (acetaminophen, dextromethorphan Hbr, Phenylephrine HCl)
Drug Information of DayRelief
| Product NDC: | 55312-656 |
| Proprietary Name: | DayRelief |
| Non Proprietary Name: | acetaminophen, dextromethorphan Hbr, Phenylephrine HCl |
| Active Ingredient(s): | 325; 10; 5 mg/15mL; mg/15mL; mg/15mL & nbsp; acetaminophen, dextromethorphan Hbr, Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DayRelief
| Product NDC: | 55312-656 |
| Labeler Name: | Western Family Foods Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060705 |
Package Information of DayRelief
| Package NDC: | 55312-656-30 |
| Package Description: | 177 mL in 1 BOTTLE (55312-656-30) |
NDC Information of DayRelief
| NDC Code | 55312-656-30 |
| Proprietary Name | DayRelief |
| Package Description | 177 mL in 1 BOTTLE (55312-656-30) |
| Product NDC | 55312-656 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen, dextromethorphan Hbr, Phenylephrine HCl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20060705 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Western Family Foods Inc |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 5 |
| Strength Unit | mg/15mL; mg/15mL; mg/15mL |
| Pharmaceutical Classes |
