| Product NDC: | 75847-1601 |
| Proprietary Name: | DR. IASO |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 7.5 mL/100mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 75847-1601 |
| Labeler Name: | IASO Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120617 |
| Package NDC: | 75847-1601-1 |
| Package Description: | 60 mL in 1 BOTTLE, PLASTIC (75847-1601-1) |
| NDC Code | 75847-1601-1 |
| Proprietary Name | DR. IASO |
| Package Description | 60 mL in 1 BOTTLE, PLASTIC (75847-1601-1) |
| Product NDC | 75847-1601 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120617 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | IASO Inc |
| Substance Name | OCTINOXATE |
| Strength Number | 7.5 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |