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Daytime Multi-Symptom Cold Relief - 50844-470-02 - (Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl)

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Drug Information of Daytime Multi-Symptom Cold Relief

Product NDC: 50844-470
Proprietary Name: Daytime Multi-Symptom Cold Relief
Non Proprietary Name: Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl
Active Ingredient(s): 325; 10; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Daytime Multi-Symptom Cold Relief

Product NDC: 50844-470
Labeler Name: L.N.K. International, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20050715

Package Information of Daytime Multi-Symptom Cold Relief

Package NDC: 50844-470-02
Package Description: 1 BLISTER PACK in 1 BOX (50844-470-02) > 12 TABLET in 1 BLISTER PACK

NDC Information of Daytime Multi-Symptom Cold Relief

NDC Code 50844-470-02
Proprietary Name Daytime Multi-Symptom Cold Relief
Package Description 1 BLISTER PACK in 1 BOX (50844-470-02) > 12 TABLET in 1 BLISTER PACK
Product NDC 50844-470
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050715
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name L.N.K. International, Inc.
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Daytime Multi-Symptom Cold Relief


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