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Hemo Fin
Hemo Fin - 50211-001-01 - (Petrolatum)
Drug Information of Hemo Fin
| Product NDC: | 50211-001 |
| Proprietary Name: | Hemo Fin |
| Non Proprietary Name: | Petrolatum |
| Active Ingredient(s): | 93.3 g/100g & nbsp; Petrolatum |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hemo Fin
| Product NDC: | 50211-001 |
| Labeler Name: | PD MERC LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120910 |
Package Information of Hemo Fin
| Package NDC: | 50211-001-01 |
| Package Description: | 28 g in 1 TUBE, WITH APPLICATOR (50211-001-01) |
NDC Information of Hemo Fin
| NDC Code | 50211-001-01 |
| Proprietary Name | Hemo Fin |
| Package Description | 28 g in 1 TUBE, WITH APPLICATOR (50211-001-01) |
| Product NDC | 50211-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Petrolatum |
| Dosage Form Name | OINTMENT |
| Route Name | RECTAL |
| Start Marketing Date | 20120910 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | PD MERC LLC |
| Substance Name | PETROLATUM |
| Strength Number | 93.3 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
