| Product NDC: | 62032-512 |
| Proprietary Name: | CLENZIDERM NORMAL TO DRY SKIN |
| Non Proprietary Name: | GLYCERIN AND BENZOYL PEROXIDE |
| Active Ingredient(s): | & nbsp; GLYCERIN AND BENZOYL PEROXIDE |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62032-512 |
| Labeler Name: | OMP, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20070701 |
| Package NDC: | 62032-512-03 |
| Package Description: | 1 KIT in 1 CARTON (62032-512-03) * 47 mL in 1 BOTTLE, PLASTIC (62032-113-65) * 192 mL in 1 BOTTLE, PLASTIC * 50 mL in 1 BOTTLE, PLASTIC (62032-114-70) |
| NDC Code | 62032-512-03 |
| Proprietary Name | CLENZIDERM NORMAL TO DRY SKIN |
| Package Description | 1 KIT in 1 CARTON (62032-512-03) * 47 mL in 1 BOTTLE, PLASTIC (62032-113-65) * 192 mL in 1 BOTTLE, PLASTIC * 50 mL in 1 BOTTLE, PLASTIC (62032-114-70) |
| Product NDC | 62032-512 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GLYCERIN AND BENZOYL PEROXIDE |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20070701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | OMP, INC. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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