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: | 14783-770-04 |
Package Description: | 1 BOTTLE in 1 CARTON (14783-770-04) > 3 g in 1 BOTTLE (14783-770-03) |
NDC Code | 14783-770-04 |
Proprietary Name | LBEL Effet Parfait Mineral Natural Skin Effect Mouse Foundation |
Package Description | 1 BOTTLE in 1 CARTON (14783-770-04) > 3 g in 1 BOTTLE (14783-770-03) |
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 |