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Clearasil Ultra Rapid Action
Clearasil Ultra Rapid Action - 63824-305-65 - (Salicylic Acid)
Drug Information of Clearasil Ultra Rapid Action
| Product NDC: | 63824-305 |
| Proprietary Name: | Clearasil Ultra Rapid Action |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | 2 g/100mL & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clearasil Ultra Rapid Action
| Product NDC: | 63824-305 |
| Labeler Name: | Reckitt Benckiser LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120925 |
Package Information of Clearasil Ultra Rapid Action
| Package NDC: | 63824-305-65 |
| Package Description: | 150 mL in 1 TUBE (63824-305-65) |
NDC Information of Clearasil Ultra Rapid Action
| NDC Code | 63824-305-65 |
| Proprietary Name | Clearasil Ultra Rapid Action |
| Package Description | 150 mL in 1 TUBE (63824-305-65) |
| Product NDC | 63824-305 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120925 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Reckitt Benckiser LLC |
| Substance Name | SALICYLIC ACID |
| Strength Number | 2 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
