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NeoBenz Micro Plus Pack
NeoBenz Micro Plus Pack - 67402-021-23 - (benzoyl peroxide)
Drug Information of NeoBenz Micro Plus Pack
| 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) |
Labeler Information of NeoBenz Micro Plus Pack
| 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 Information of NeoBenz Micro Plus Pack
| 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 Information of NeoBenz Micro Plus Pack
| 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 |
