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Day Time Cold and Flu Relief - 0904-5763-44 - (Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride)

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Drug Information of Day Time Cold and Flu Relief

Product NDC: 0904-5763
Proprietary Name: Day Time Cold and 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 Day Time Cold and Flu Relief

Product NDC: 0904-5763
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110325

Package Information of Day Time Cold and Flu Relief

Package NDC: 0904-5763-44
Package Description: 16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0904-5763-44)

NDC Information of Day Time Cold and Flu Relief

NDC Code 0904-5763-44
Proprietary Name Day Time Cold and Flu Relief
Package Description 16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0904-5763-44)
Product NDC 0904-5763
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 20110325
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Major Pharmaceuticals
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 Day Time Cold and Flu Relief


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