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OC Eight
OC Eight - 42485-003-01 - (benzoyl peroxide)
Drug Information of OC Eight
| Product NDC: | 42485-003 |
| Proprietary Name: | OC Eight |
| Non Proprietary Name: | benzoyl peroxide |
| Active Ingredient(s): | 7 mg/g & nbsp; benzoyl peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OC Eight
| Product NDC: | 42485-003 |
| Labeler Name: | Biopelle, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110401 |
Package Information of OC Eight
| Package NDC: | 42485-003-01 |
| Package Description: | 45 g in 1 TUBE (42485-003-01) |
NDC Information of OC Eight
| NDC Code | 42485-003-01 |
| Proprietary Name | OC Eight |
| Package Description | 45 g in 1 TUBE (42485-003-01) |
| Product NDC | 42485-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzoyl peroxide |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110401 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Biopelle, Inc. |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 7 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
