Product NDC: | 13537-022 |
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: | 13537-022 |
Labeler Name: | Ventura Corporation Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110810 |
Package NDC: | 13537-022-02 |
Package Description: | 1 CONTAINER in 1 CARTON (13537-022-02) > 10 g in 1 CONTAINER (13537-022-01) |
NDC Code | 13537-022-02 |
Proprietary Name | LBEL |
Package Description | 1 CONTAINER in 1 CARTON (13537-022-02) > 10 g in 1 CONTAINER (13537-022-01) |
Product NDC | 13537-022 |
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 | 20110810 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ventura Corporation Ltd. |
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 |