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PanOxyl
PanOxyl - 0145-2661-05 - (benzoyl peroxide)
Drug Information of PanOxyl
| Product NDC: | 0145-2661 |
| Proprietary Name: | PanOxyl |
| Non Proprietary Name: | benzoyl peroxide |
| Active Ingredient(s): | 117.3 mg/g & nbsp; benzoyl peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PanOxyl
| Product NDC: | 0145-2661 |
| Labeler Name: | Stiefel Laboratories Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110325 |
Package Information of PanOxyl
| Package NDC: | 0145-2661-05 |
| Package Description: | 1 TUBE in 1 CARTON (0145-2661-05) > 170.1 g in 1 TUBE |
NDC Information of PanOxyl
| NDC Code | 0145-2661-05 |
| Proprietary Name | PanOxyl |
| Package Description | 1 TUBE in 1 CARTON (0145-2661-05) > 170.1 g in 1 TUBE |
| Product NDC | 0145-2661 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzoyl peroxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110325 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Stiefel Laboratories Inc |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 117.3 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
