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PAIN RELIEVER PM - 63941-231-50 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of PAIN RELIEVER PM

Product NDC: 63941-231
Proprietary Name: PAIN RELIEVER PM
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): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of PAIN RELIEVER PM

Product NDC: 63941-231
Labeler Name: Best Choice (Valu Merchandisers Company)
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130308

Package Information of PAIN RELIEVER PM

Package NDC: 63941-231-50
Package Description: 1 BOTTLE, PLASTIC in 1 BOX (63941-231-50) > 50 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC

NDC Information of PAIN RELIEVER PM

NDC Code 63941-231-50
Proprietary Name PAIN RELIEVER PM
Package Description 1 BOTTLE, PLASTIC in 1 BOX (63941-231-50) > 50 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC
Product NDC 63941-231
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20130308
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Best Choice (Valu Merchandisers Company)
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of PAIN RELIEVER PM


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