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BPO
BPO - 42192-105-16 - (benzoyl peroxide)
Drug Information of BPO
| Product NDC: | 42192-105 |
| Proprietary Name: | BPO |
| Non Proprietary Name: | benzoyl peroxide |
| Active Ingredient(s): | 4 mg/100mg & nbsp; benzoyl peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BPO
| Product NDC: | 42192-105 |
| Labeler Name: | Acella Pharmaceuticals, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090101 |
Package Information of BPO
| Package NDC: | 42192-105-16 |
| Package Description: | 12 CARTON in 1 PACKAGE (42192-105-16) > 1 TUBE in 1 CARTON > 42500 mg in 1 TUBE |
NDC Information of BPO
| NDC Code | 42192-105-16 |
| Proprietary Name | BPO |
| Package Description | 12 CARTON in 1 PACKAGE (42192-105-16) > 1 TUBE in 1 CARTON > 42500 mg in 1 TUBE |
| Product NDC | 42192-105 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzoyl peroxide |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20090101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Acella Pharmaceuticals, LLC |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 4 |
| Strength Unit | mg/100mg |
| Pharmaceutical Classes |
