| Product NDC: | 14783-434 |
| Proprietary Name: | LBEL |
| Non Proprietary Name: | Avobenzone, Ensulizole, Octisalate, Octocrylene, and Oxybenzone |
| Active Ingredient(s): | .03; .03; .05; .05; .06 g/mL; g/mL; g/mL; g/mL; g/mL & nbsp; Avobenzone, Ensulizole, Octisalate, Octocrylene, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 14783-434 |
| Labeler Name: | Ventura International Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111126 |
| Package NDC: | 14783-434-04 |
| Package Description: | 1 BOTTLE in 1 BOX (14783-434-04) > 3 mL in 1 BOTTLE |
| NDC Code | 14783-434-04 |
| Proprietary Name | LBEL |
| Package Description | 1 BOTTLE in 1 BOX (14783-434-04) > 3 mL in 1 BOTTLE |
| Product NDC | 14783-434 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Ensulizole, Octisalate, Octocrylene, and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20111126 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ventura International Ltd. |
| Substance Name | AVOBENZONE; ENSULIZOLE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | .03; .03; .05; .05; .06 |
| Strength Unit | g/mL; g/mL; g/mL; g/mL; g/mL |
| Pharmaceutical Classes |