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Clearasil Ultra
Clearasil Ultra - 63824-345-01 - (Salicylic Acid)
Drug Information of Clearasil Ultra
| Product NDC: | 63824-345 |
| Proprietary Name: | Clearasil Ultra |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | .03 g/1 & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clearasil Ultra
| Product NDC: | 63824-345 |
| Labeler Name: | Reckitt Benckiser LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111212 |
Package Information of Clearasil Ultra
| Package NDC: | 63824-345-01 |
| Package Description: | 90 SOLUTION in 1 JAR (63824-345-01) |
NDC Information of Clearasil Ultra
| NDC Code | 63824-345-01 |
| Proprietary Name | Clearasil Ultra |
| Package Description | 90 SOLUTION in 1 JAR (63824-345-01) |
| Product NDC | 63824-345 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20111212 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Reckitt Benckiser LLC |
| Substance Name | SALICYLIC ACID |
| Strength Number | .03 |
| Strength Unit | g/1 |
| Pharmaceutical Classes |
