Product NDC: | 50580-403 |
Proprietary Name: | TYLENOL Cold and Flu Severe |
Non Proprietary Name: | Acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride |
Active Ingredient(s): | 325; 10; 200; 5 mg/15mL; mg/15mL; mg/15mL; mg/15mL & nbsp; Acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50580-403 |
Labeler Name: | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100705 |
Package NDC: | 50580-403-08 |
Package Description: | 240 mL in 1 BOTTLE, PLASTIC (50580-403-08) |
NDC Code | 50580-403-08 |
Proprietary Name | TYLENOL Cold and Flu Severe |
Package Description | 240 mL in 1 BOTTLE, PLASTIC (50580-403-08) |
Product NDC | 50580-403 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20100705 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 10; 200; 5 |
Strength Unit | mg/15mL; mg/15mL; mg/15mL; mg/15mL |
Pharmaceutical Classes |