Product NDC: | 43596-0001 |
Proprietary Name: | LBEL DEFENSE 365 Daily Protective Facial SPF 50 |
Non Proprietary Name: | HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
Active Ingredient(s): | 5; 7; 5; 4; 6.24; 3.92 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43596-0001 |
Labeler Name: | Ventura Corporation, LTD |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120325 |
Package NDC: | 43596-0001-1 |
Package Description: | 3 mL in 1 TUBE (43596-0001-1) |
NDC Code | 43596-0001-1 |
Proprietary Name | LBEL DEFENSE 365 Daily Protective Facial SPF 50 |
Package Description | 3 mL in 1 TUBE (43596-0001-1) |
Product NDC | 43596-0001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120325 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Ventura Corporation, LTD |
Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 5; 7; 5; 4; 6.24; 3.92 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |