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PRAX
PRAX - 0496-0748-15 - (pramoxine hydrochloride)
Drug Information of PRAX
| 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) |
Labeler Information of PRAX
| 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 Information of PRAX
| Package NDC: | 0496-0748-15 |
| Package Description: | 15 mL in 1 BOTTLE (0496-0748-15) |
NDC Information of PRAX
| NDC Code | 0496-0748-15 |
| Proprietary Name | PRAX |
| Package Description | 15 mL in 1 BOTTLE (0496-0748-15) |
| 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 |
