| Product NDC: | 13537-230 |
| Proprietary Name: | LBel |
| Non Proprietary Name: | Octinoxate |
| Active Ingredient(s): | 2.1 g/30mL & nbsp; Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 13537-230 |
| Labeler Name: | VENTURA INTERNATIONAL LTD., |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100815 |
| Package NDC: | 13537-230-62 |
| Package Description: | 1 BOTTLE in 1 BOX (13537-230-62) > 30 mL in 1 BOTTLE (13537-230-61) |
| NDC Code | 13537-230-62 |
| Proprietary Name | LBel |
| Package Description | 1 BOTTLE in 1 BOX (13537-230-62) > 30 mL in 1 BOTTLE (13537-230-61) |
| Product NDC | 13537-230 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100815 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | VENTURA INTERNATIONAL LTD., |
| Substance Name | OCTINOXATE |
| Strength Number | 2.1 |
| Strength Unit | g/30mL |
| Pharmaceutical Classes |