| Product NDC: | 75847-7001 |
| Proprietary Name: | IASO Intensive Clear Booster |
| Non Proprietary Name: | SALICYLIC ACID |
| Active Ingredient(s): | .003 mL/mL & nbsp; SALICYLIC ACID |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 75847-7001 |
| Labeler Name: | IASO Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110109 |
| Package NDC: | 75847-7001-1 |
| Package Description: | 35 mL in 1 BOTTLE, WITH APPLICATOR (75847-7001-1) |
| NDC Code | 75847-7001-1 |
| Proprietary Name | IASO Intensive Clear Booster |
| Package Description | 35 mL in 1 BOTTLE, WITH APPLICATOR (75847-7001-1) |
| Product NDC | 75847-7001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SALICYLIC ACID |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110109 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | IASO Inc |
| Substance Name | SALICYLIC ACID |
| Strength Number | .003 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |