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Proctofoam
Proctofoam - 68220-143-15 - (pramoxine hydrochloride)
Drug Information of Proctofoam
| Product NDC: | 68220-143 |
| Proprietary Name: | Proctofoam |
| Non Proprietary Name: | pramoxine hydrochloride |
| Active Ingredient(s): | 150 mg/15g & nbsp; pramoxine hydrochloride |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Proctofoam
| Product NDC: | 68220-143 |
| Labeler Name: | Alaven Pharmaceutical LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19900930 |
Package Information of Proctofoam
| Package NDC: | 68220-143-15 |
| Package Description: | 1 CONTAINER in 1 CARTON (68220-143-15) > 15 g in 1 CONTAINER |
NDC Information of Proctofoam
| NDC Code | 68220-143-15 |
| Proprietary Name | Proctofoam |
| Package Description | 1 CONTAINER in 1 CARTON (68220-143-15) > 15 g in 1 CONTAINER |
| Product NDC | 68220-143 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | pramoxine hydrochloride |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | RECTAL |
| Start Marketing Date | 19900930 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Alaven Pharmaceutical LLC |
| Substance Name | PRAMOXINE HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/15g |
| Pharmaceutical Classes |
