| Product NDC: | 60681-5604 |
| Proprietary Name: | Pleo Usti |
| Non Proprietary Name: | ustilago maydis |
| Active Ingredient(s): | 5 [HP_X]/1 & nbsp; ustilago maydis |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 60681-5604 |
| Labeler Name: | Sanum Kehlbeck GmbH & Co. KG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20040421 |
| Package NDC: | 60681-5604-1 |
| Package Description: | 1 DOSE PACK in 1 CARTON (60681-5604-1) > 10 SUPPOSITORY in 1 DOSE PACK |
| NDC Code | 60681-5604-1 |
| Proprietary Name | Pleo Usti |
| Package Description | 1 DOSE PACK in 1 CARTON (60681-5604-1) > 10 SUPPOSITORY in 1 DOSE PACK |
| Product NDC | 60681-5604 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ustilago maydis |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 20040421 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Sanum Kehlbeck GmbH & Co. KG |
| Substance Name | USTILAGO MAYDIS |
| Strength Number | 5 |
| Strength Unit | [HP_X]/1 |
| Pharmaceutical Classes |