Hemorrhoid - 50114-8006-8 - (PAEONIA OFFICINALIS ROOT)

Alphabetical Index


Drug Information of Hemorrhoid

Product NDC: 50114-8006
Proprietary Name: Hemorrhoid
Non Proprietary Name: PAEONIA OFFICINALIS ROOT
Active Ingredient(s): 1    [hp_X]/50g & nbsp;   PAEONIA OFFICINALIS ROOT
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Hemorrhoid

Product NDC: 50114-8006
Labeler Name: Heel Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20000131

Package Information of Hemorrhoid

Package NDC: 50114-8006-8
Package Description: 1 TUBE in 1 CARTON (50114-8006-8) > 50 g in 1 TUBE

NDC Information of Hemorrhoid

NDC Code 50114-8006-8
Proprietary Name Hemorrhoid
Package Description 1 TUBE in 1 CARTON (50114-8006-8) > 50 g in 1 TUBE
Product NDC 50114-8006
Product Type Name HUMAN OTC DRUG
Non Proprietary Name PAEONIA OFFICINALIS ROOT
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20000131
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Heel Inc
Substance Name PAEONIA OFFICINALIS ROOT
Strength Number 1
Strength Unit [hp_X]/50g
Pharmaceutical Classes

Complete Information of Hemorrhoid


General Information