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Denorex Extra Strength
Denorex Extra Strength - 51545-210-12 - (Salicylic Acid)
Drug Information of Denorex Extra Strength
| Product NDC: | 51545-210 |
| Proprietary Name: | Denorex Extra Strength |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | .03 g/mL & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Denorex Extra Strength
| Product NDC: | 51545-210 |
| Labeler Name: | Ultimark Products LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091101 |
Package Information of Denorex Extra Strength
| Package NDC: | 51545-210-12 |
| Package Description: | 296 mL in 1 BOTTLE (51545-210-12) |
NDC Information of Denorex Extra Strength
| NDC Code | 51545-210-12 |
| Proprietary Name | Denorex Extra Strength |
| Package Description | 296 mL in 1 BOTTLE (51545-210-12) |
| Product NDC | 51545-210 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20091101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ultimark Products LLC |
| Substance Name | SALICYLIC ACID |
| Strength Number | .03 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
