| Product NDC: | 14783-072 |
| Proprietary Name: | LBel |
| Non Proprietary Name: | Ensulizole, Octinoxate, and Oxybenzone |
| Active Ingredient(s): | 3; 7.5; 6.2 g/100mL; g/100mL; g/100mL & nbsp; Ensulizole, Octinoxate, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 14783-072 |
| 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: | 14783-072-61 |
| Package Description: | 1 JAR in 1 BOX (14783-072-61) > 100 mL in 1 JAR (14783-072-62) |
| NDC Code | 14783-072-61 |
| Proprietary Name | LBel |
| Package Description | 1 JAR in 1 BOX (14783-072-61) > 100 mL in 1 JAR (14783-072-62) |
| Product NDC | 14783-072 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ensulizole, Octinoxate, and Oxybenzone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100815 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | VENTURA INTERNATIONAL LTD., |
| Substance Name | ENSULIZOLE; OCTINOXATE; OXYBENZONE |
| Strength Number | 3; 7.5; 6.2 |
| Strength Unit | g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |