Fem Relief - 0498-7000-50 - (Acetaminophen Pamabrom)

Alphabetical Index


Drug Information of Fem Relief

Product NDC: 0498-7000
Proprietary Name: Fem Relief
Non Proprietary Name: Acetaminophen Pamabrom
Active Ingredient(s): 325; 25    mg/1; mg/1 & nbsp;   Acetaminophen Pamabrom
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fem Relief

Product NDC: 0498-7000
Labeler Name: North Safety Products LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120215

Package Information of Fem Relief

Package NDC: 0498-7000-50
Package Description: 250 BOX in 1 BOX (0498-7000-50) > 125 BOX in 1 BOX (0498-7000-25) > 50 PACKET in 1 BOX (0498-7000-10) > 2 TABLET in 1 PACKET (0498-7000-01)

NDC Information of Fem Relief

NDC Code 0498-7000-50
Proprietary Name Fem Relief
Package Description 250 BOX in 1 BOX (0498-7000-50) > 125 BOX in 1 BOX (0498-7000-25) > 50 PACKET in 1 BOX (0498-7000-10) > 2 TABLET in 1 PACKET (0498-7000-01)
Product NDC 0498-7000
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen Pamabrom
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120215
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name North Safety Products LLC
Substance Name ACETAMINOPHEN; PAMABROM
Strength Number 325; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Fem Relief


General Information