Product NDC: | 0496-0748 |
Proprietary Name: | PRAX |
Non Proprietary Name: | pramoxine hydrochloride |
Active Ingredient(s): | 10 mg/mL & nbsp; pramoxine hydrochloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0496-0748 |
Labeler Name: | Ferndale Laboratories, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part346 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120401 |
Package NDC: | 0496-0748-04 |
Package Description: | 118 mL in 1 BOTTLE (0496-0748-04) |
NDC Code | 0496-0748-04 |
Proprietary Name | PRAX |
Package Description | 118 mL in 1 BOTTLE (0496-0748-04) |
Product NDC | 0496-0748 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | pramoxine hydrochloride |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120401 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Ferndale Laboratories, Inc. |
Substance Name | PRAMOXINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes |