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Daytime Cold Flu Relief - 59779-472-36 - (Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride)

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Drug Information of Daytime Cold Flu Relief

Product NDC: 59779-472
Proprietary Name: Daytime Cold Flu Relief
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Active Ingredient(s): 325; 10; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Daytime Cold Flu Relief

Product NDC: 59779-472
Labeler Name: CVS Pharmacy
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130531

Package Information of Daytime Cold Flu Relief

Package NDC: 59779-472-36
Package Description: 3 BLISTER PACK in 1 CARTON (59779-472-36) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Daytime Cold Flu Relief

NDC Code 59779-472-36
Proprietary Name Daytime Cold Flu Relief
Package Description 3 BLISTER PACK in 1 CARTON (59779-472-36) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 59779-472
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20130531
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name CVS Pharmacy
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 Cold Flu Relief


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