Product NDC: | 41163-201 |
Proprietary Name: | Day Time with PE |
Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride |
Active Ingredient(s): | 325; 10; 5 mg/15mL; mg/15mL; mg/15mL & nbsp; Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41163-201 |
Labeler Name: | Supervalu |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090320 |
Package NDC: | 41163-201-16 |
Package Description: | 177 mL in 1 BOTTLE, PLASTIC (41163-201-16) |
NDC Code | 41163-201-16 |
Proprietary Name | Day Time with PE |
Package Description | 177 mL in 1 BOTTLE, PLASTIC (41163-201-16) |
Product NDC | 41163-201 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20090320 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Supervalu |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 10; 5 |
Strength Unit | mg/15mL; mg/15mL; mg/15mL |
Pharmaceutical Classes |