| Product NDC: | 66993-928 |
| Proprietary Name: | Lavoclen |
| Non Proprietary Name: | benzoyl peroxide |
| Active Ingredient(s): | 6.8 g/170.1g & nbsp; benzoyl peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 66993-928 |
| Labeler Name: | Prasco Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090701 |
| Package NDC: | 66993-928-98 |
| Package Description: | 170.1 g in 1 TUBE (66993-928-98) |
| NDC Code | 66993-928-98 |
| Proprietary Name | Lavoclen |
| Package Description | 170.1 g in 1 TUBE (66993-928-98) |
| Product NDC | 66993-928 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | benzoyl peroxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Prasco Laboratories |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 6.8 |
| Strength Unit | g/170.1g |
| Pharmaceutical Classes |