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Medi-First Plus Cold Relief - 47682-922-48 - (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE)

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Drug Information of Medi-First Plus Cold Relief

Product NDC: 47682-922
Proprietary Name: Medi-First Plus Cold Relief
Non Proprietary Name: ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Active Ingredient(s): 325; 15; 200; 5    mg/1; mg/1; mg/1; mg/1 & nbsp;   ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Medi-First Plus Cold Relief

Product NDC: 47682-922
Labeler Name: Unifirst First Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20081230

Package Information of Medi-First Plus Cold Relief

Package NDC: 47682-922-48
Package Description: 125 PACKET in 1 BOX, UNIT-DOSE (47682-922-48) > 2 TABLET, FILM COATED in 1 PACKET

NDC Information of Medi-First Plus Cold Relief

NDC Code 47682-922-48
Proprietary Name Medi-First Plus Cold Relief
Package Description 125 PACKET in 1 BOX, UNIT-DOSE (47682-922-48) > 2 TABLET, FILM COATED in 1 PACKET
Product NDC 47682-922
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081230
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Unifirst First Aid Corporation
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 15; 200; 5
Strength Unit mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Medi-First Plus Cold Relief


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