| Product NDC: | 14783-770 |
| Proprietary Name: | LBEL Effet Parfait Mineral Natural Skin Effect Mouse Foundation |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | .065; .024; .016 g/g; g/g; g/g & nbsp; OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 14783-770 |
| Labeler Name: | Ventura International, Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101126 |
| Package NDC: | 14783-770-31 |
| Package Description: | 1 BOTTLE in 1 CARTON (14783-770-31) > 30 g in 1 BOTTLE (14783-770-30) |
| NDC Code | 14783-770-31 |
| Proprietary Name | LBEL Effet Parfait Mineral Natural Skin Effect Mouse Foundation |
| Package Description | 1 BOTTLE in 1 CARTON (14783-770-31) > 30 g in 1 BOTTLE (14783-770-30) |
| Product NDC | 14783-770 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20101126 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ventura International, Limited |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .065; .024; .016 |
| Strength Unit | g/g; g/g; g/g |
| Pharmaceutical Classes |