| Product NDC: | 42192-119 |
| Proprietary Name: | hydrocortisone acetate pramoxine hcl |
| Non Proprietary Name: | hydrocortisone acetate pramoxine hcl |
| Active Ingredient(s): | & nbsp; hydrocortisone acetate pramoxine hcl |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42192-119 |
| Labeler Name: | Acella Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100201 |
| Package NDC: | 42192-119-30 |
| Package Description: | 1 KIT in 1 CARTON (42192-119-30) * 4 g in 1 TUBE, WITH APPLICATOR * 6 g in 1 POUCH |
| NDC Code | 42192-119-30 |
| Proprietary Name | hydrocortisone acetate pramoxine hcl |
| Package Description | 1 KIT in 1 CARTON (42192-119-30) * 4 g in 1 TUBE, WITH APPLICATOR * 6 g in 1 POUCH |
| Product NDC | 42192-119 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocortisone acetate pramoxine hcl |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20100201 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Acella Pharmaceuticals, LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |