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rx act Pain Relief - 37808-437-71 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of rx act Pain Relief

Product NDC: 37808-437
Proprietary Name: rx act 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 rx act Pain Relief

Product NDC: 37808-437
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19960710

Package Information of rx act Pain Relief

Package NDC: 37808-437-71
Package Description: 1 BOTTLE in 1 CARTON (37808-437-71) > 50 TABLET, FILM COATED in 1 BOTTLE

NDC Information of rx act Pain Relief

NDC Code 37808-437-71
Proprietary Name rx act Pain Relief
Package Description 1 BOTTLE in 1 CARTON (37808-437-71) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC 37808-437
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19960710
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H E B
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of rx act Pain Relief


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