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TYLENOL COLD
TYLENOL COLD - 50580-349-08 - (Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride)
Drug Information of TYLENOL COLD
| Product NDC: | 50580-349 |
| Proprietary Name: | TYLENOL COLD |
| 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) |
Labeler Information of TYLENOL COLD
| Product NDC: | 50580-349 |
| 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: | 20080701 |
Package Information of TYLENOL COLD
| Package NDC: | 50580-349-08 |
| Package Description: | 240 mL in 1 BOTTLE, PLASTIC (50580-349-08) |
NDC Information of TYLENOL COLD
| NDC Code | 50580-349-08 |
| Proprietary Name | TYLENOL COLD |
| Package Description | 240 mL in 1 BOTTLE, PLASTIC (50580-349-08) |
| Product NDC | 50580-349 |
| 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 | 20080701 |
| 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 |
