Product NDC: | 67402-021 |
Proprietary Name: | NeoBenz Micro Plus Pack |
Non Proprietary Name: | benzoyl peroxide |
Active Ingredient(s): | & nbsp; benzoyl peroxide |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67402-021 |
Labeler Name: | SkinMedica Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20090416 |
Package NDC: | 67402-021-23 |
Package Description: | 1 KIT in 1 BOX (67402-021-23) * 45 g in 1 TUBE * 7 POUCH in 1 CASE (67402-023-07) > .5 g in 1 POUCH (67402-023-01) |
NDC Code | 67402-021-23 |
Proprietary Name | NeoBenz Micro Plus Pack |
Package Description | 1 KIT in 1 BOX (67402-021-23) * 45 g in 1 TUBE * 7 POUCH in 1 CASE (67402-023-07) > .5 g in 1 POUCH (67402-023-01) |
Product NDC | 67402-021 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | benzoyl peroxide |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20090416 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | SkinMedica Pharmaceuticals, Inc. |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |