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PROCORT
PROCORT - 50967-357-60 - (1.85% hydrocortisone acetate - 1.15% pramoxine hci cream)
Drug Information of PROCORT
| Product NDC: | 50967-357 |
| Proprietary Name: | PROCORT |
| Non Proprietary Name: | 1.85% hydrocortisone acetate - 1.15% pramoxine hci cream |
| Active Ingredient(s): | 18.5; 11.5 mg/g; mg/g & nbsp; 1.85% hydrocortisone acetate - 1.15% pramoxine hci cream |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PROCORT
| Product NDC: | 50967-357 |
| Labeler Name: | Womens Choice Pharmaceuticals LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110630 |
Package Information of PROCORT
| Package NDC: | 50967-357-60 |
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (50967-357-60) > 1 TUBE, WITH APPLICATOR in 1 TUBE, WITH APPLICATOR > 60 g in 1 TUBE, WITH APPLICATOR |
NDC Information of PROCORT
| NDC Code | 50967-357-60 |
| Proprietary Name | PROCORT |
| Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (50967-357-60) > 1 TUBE, WITH APPLICATOR in 1 TUBE, WITH APPLICATOR > 60 g in 1 TUBE, WITH APPLICATOR |
| Product NDC | 50967-357 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | 1.85% hydrocortisone acetate - 1.15% pramoxine hci cream |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110630 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Womens Choice Pharmaceuticals LLC |
| Substance Name | HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 18.5; 11.5 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
