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Pain Relief - 42507-437-71 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of Pain Relief

Product NDC: 42507-437
Proprietary Name: Pain Relief
Non Proprietary Name: Acetaminophen, Diphenhydramine HCl
Active Ingredient(s): 500; 25    mg/1; mg/1 & nbsp;   Acetaminophen, Diphenhydramine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Pain Relief

Product NDC: 42507-437
Labeler Name: HyVee Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19921119

Package Information of Pain Relief

Package NDC: 42507-437-71
Package Description: 1 BOTTLE in 1 CARTON (42507-437-71) > 50 TABLET, FILM COATED in 1 BOTTLE

NDC Information of Pain Relief

NDC Code 42507-437-71
Proprietary Name Pain Relief
Package Description 1 BOTTLE in 1 CARTON (42507-437-71) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC 42507-437
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19921119
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name HyVee Inc
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Pain Relief


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