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CLENZIDERM PORE THERAPY
CLENZIDERM PORE THERAPY - 62032-110-60 - (SALICYLIC ACID)
Drug Information of CLENZIDERM PORE THERAPY
| Product NDC: | 62032-110 |
| Proprietary Name: | CLENZIDERM PORE THERAPY |
| Non Proprietary Name: | SALICYLIC ACID |
| Active Ingredient(s): | 20 mg/mL & nbsp; SALICYLIC ACID |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CLENZIDERM PORE THERAPY
| Product NDC: | 62032-110 |
| Labeler Name: | OMP, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20070201 |
Package Information of CLENZIDERM PORE THERAPY
| Package NDC: | 62032-110-60 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (62032-110-60) |
NDC Information of CLENZIDERM PORE THERAPY
| NDC Code | 62032-110-60 |
| Proprietary Name | CLENZIDERM PORE THERAPY |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (62032-110-60) |
| Product NDC | 62032-110 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SALICYLIC ACID |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20070201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | OMP, INC. |
| Substance Name | SALICYLIC ACID |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
