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CLENZIDERM THERAPEUTIC
CLENZIDERM THERAPEUTIC - 62032-113-65 - (BENZOYL PEROXIDE)
Drug Information of CLENZIDERM THERAPEUTIC
| Product NDC: | 62032-113 |
| Proprietary Name: | CLENZIDERM THERAPEUTIC |
| Non Proprietary Name: | BENZOYL PEROXIDE |
| Active Ingredient(s): | 50 mg/mL & nbsp; BENZOYL PEROXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CLENZIDERM THERAPEUTIC
| Product NDC: | 62032-113 |
| Labeler Name: | OMP, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20070701 |
Package Information of CLENZIDERM THERAPEUTIC
| Package NDC: | 62032-113-65 |
| Package Description: | 47 mL in 1 BOTTLE, PLASTIC (62032-113-65) |
NDC Information of CLENZIDERM THERAPEUTIC
| NDC Code | 62032-113-65 |
| Proprietary Name | CLENZIDERM THERAPEUTIC |
| Package Description | 47 mL in 1 BOTTLE, PLASTIC (62032-113-65) |
| Product NDC | 62032-113 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZOYL PEROXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20070701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | OMP, INC. |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
