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TYLENOL COLD MULTI-SYMPTOM DAYTIME - 50580-257-08 - (Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride)

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Drug Information of TYLENOL COLD MULTI-SYMPTOM DAYTIME

Product NDC: 50580-257
Proprietary Name: TYLENOL COLD MULTI-SYMPTOM DAYTIME
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)

Labeler Information of TYLENOL COLD MULTI-SYMPTOM DAYTIME

Product NDC: 50580-257
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: 20060701

Package Information of TYLENOL COLD MULTI-SYMPTOM DAYTIME

Package NDC: 50580-257-08
Package Description: 240 mL in 1 BOTTLE, PLASTIC (50580-257-08)

NDC Information of TYLENOL COLD MULTI-SYMPTOM DAYTIME

NDC Code 50580-257-08
Proprietary Name TYLENOL COLD MULTI-SYMPTOM DAYTIME
Package Description 240 mL in 1 BOTTLE, PLASTIC (50580-257-08)
Product NDC 50580-257
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 20060701
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 5
Strength Unit mg/15mL; mg/15mL; mg/15mL
Pharmaceutical Classes

Complete Information of TYLENOL COLD MULTI-SYMPTOM DAYTIME


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