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Revitol
Revitol - 24488-004-20 - (Benzoyl Peroxide)
Drug Information of Revitol
| Product NDC: | 24488-004 |
| Proprietary Name: | Revitol |
| Non Proprietary Name: | Benzoyl Peroxide |
| Active Ingredient(s): | 2.95 mL/59mL & nbsp; Benzoyl Peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Revitol
| Product NDC: | 24488-004 |
| Labeler Name: | Revitol Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110414 |
Package Information of Revitol
| Package NDC: | 24488-004-20 |
| Package Description: | 59 mL in 1 JAR (24488-004-20) |
NDC Information of Revitol
| NDC Code | 24488-004-20 |
| Proprietary Name | Revitol |
| Package Description | 59 mL in 1 JAR (24488-004-20) |
| Product NDC | 24488-004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzoyl Peroxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110414 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Revitol Corporation |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 2.95 |
| Strength Unit | mL/59mL |
| Pharmaceutical Classes |
