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Complete Menstrual Relief - 50804-183-24 - (Acetaminophen, Caffeine, Pyrilamine maleate)

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Drug Information of Complete Menstrual Relief

Product NDC: 50804-183
Proprietary Name: Complete Menstrual Relief
Non Proprietary Name: Acetaminophen, Caffeine, Pyrilamine maleate
Active Ingredient(s): 500; 60; 15    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Caffeine, Pyrilamine maleate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Complete Menstrual Relief

Product NDC: 50804-183
Labeler Name: Geiss, Destin & Dunn, Inc (Goodsense)
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120116

Package Information of Complete Menstrual Relief

Package NDC: 50804-183-24
Package Description: 2 BLISTER PACK in 1 BOX (50804-183-24) > 12 TABLET in 1 BLISTER PACK

NDC Information of Complete Menstrual Relief

NDC Code 50804-183-24
Proprietary Name Complete Menstrual Relief
Package Description 2 BLISTER PACK in 1 BOX (50804-183-24) > 12 TABLET in 1 BLISTER PACK
Product NDC 50804-183
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Caffeine, Pyrilamine maleate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120116
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Geiss, Destin & Dunn, Inc (Goodsense)
Substance Name ACETAMINOPHEN; CAFFEINE; PYRILAMINE MALEATE
Strength Number 500; 60; 15
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Complete Menstrual Relief


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