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