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Tucks - 42002-504-01 - (Pramoxine Hydrochloride)
Drug Information of Tucks
| Product NDC: | 42002-504 |
| Proprietary Name: | Tucks |
| Non Proprietary Name: | Pramoxine Hydrochloride |
| Active Ingredient(s): | 10 mg/mL & nbsp; Pramoxine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tucks
| Product NDC: | 42002-504 |
| Labeler Name: | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120417 |
Package Information of Tucks
| Package NDC: | 42002-504-01 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (42002-504-01) > 14.8 mL in 1 BOTTLE, SPRAY |
NDC Information of Tucks
| NDC Code | 42002-504-01 |
| Proprietary Name | Tucks |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (42002-504-01) > 14.8 mL in 1 BOTTLE, SPRAY |
| Product NDC | 42002-504 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pramoxine Hydrochloride |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20120417 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
| Substance Name | PRAMOXINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
