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 |