| Product NDC: | 14783-013 |
| Proprietary Name: | LBEL |
| Non Proprietary Name: | TITANIUM DIOXIDE, OXYBENZONE, ZINC OXIDE, and OCTINOXATE |
| Active Ingredient(s): | .035; .05; .06; .049 g/g; g/g; g/g; g/g & nbsp; TITANIUM DIOXIDE, OXYBENZONE, ZINC OXIDE, and OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 14783-013 |
| Labeler Name: | Ventura International, Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101215 |
| Package NDC: | 14783-013-11 |
| Package Description: | 1 CONTAINER in 1 CARTON (14783-013-11) > 10 g in 1 CONTAINER (14783-013-10) |
| NDC Code | 14783-013-11 |
| Proprietary Name | LBEL |
| Package Description | 1 CONTAINER in 1 CARTON (14783-013-11) > 10 g in 1 CONTAINER (14783-013-10) |
| Product NDC | 14783-013 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE, OXYBENZONE, ZINC OXIDE, and OCTINOXATE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20101215 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ventura International, Limited |
| Substance Name | OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .035; .05; .06; .049 |
| Strength Unit | g/g; g/g; g/g; g/g |
| Pharmaceutical Classes |