| Product NDC: | 10812-279 |
| Proprietary Name: | Neutrogena SkinID |
| Non Proprietary Name: | Benzoyl Peroxide |
| Active Ingredient(s): | 35 mg/mL & nbsp; Benzoyl Peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10812-279 |
| Labeler Name: | Neutrogena Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100520 |
| Package NDC: | 10812-279-01 |
| Package Description: | 118 mL in 1 TUBE (10812-279-01) |
| NDC Code | 10812-279-01 |
| Proprietary Name | Neutrogena SkinID |
| Package Description | 118 mL in 1 TUBE (10812-279-01) |
| Product NDC | 10812-279 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzoyl Peroxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100520 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Neutrogena Corporation |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 35 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |