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 |