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OXY Clinical Foaming Face Wash
OXY Clinical Foaming Face Wash - 10742-8218-1 - (Salicylic Acid)
Drug Information of OXY Clinical Foaming Face Wash
| Product NDC: | 10742-8218 |
| Proprietary Name: | OXY Clinical Foaming Face Wash |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | 20 mg/mL & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OXY Clinical Foaming Face Wash
| Product NDC: | 10742-8218 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110516 |
Package Information of OXY Clinical Foaming Face Wash
| Package NDC: | 10742-8218-1 |
| Package Description: | 148 mL in 1 BOTTLE (10742-8218-1) |
NDC Information of OXY Clinical Foaming Face Wash
| NDC Code | 10742-8218-1 |
| Proprietary Name | OXY Clinical Foaming Face Wash |
| Package Description | 148 mL in 1 BOTTLE (10742-8218-1) |
| Product NDC | 10742-8218 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110516 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | SALICYLIC ACID |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
