Product NDC: | 43596-0006 |
Proprietary Name: | LBEL SUPREMACIE NX JOUR Replenishing Daytime Face SPF 15 Normal To Oily Skin |
Non Proprietary Name: | ENSULIZOLE, HOMOSALATE, OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE |
Active Ingredient(s): | 1.5; 1; 7.5; 4.5; 1.17 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; ENSULIZOLE, HOMOSALATE, OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43596-0006 |
Labeler Name: | Ventura Corporation, LTD |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120328 |
Package NDC: | 43596-0006-1 |
Package Description: | 5 mL in 1 TUBE (43596-0006-1) |
NDC Code | 43596-0006-1 |
Proprietary Name | LBEL SUPREMACIE NX JOUR Replenishing Daytime Face SPF 15 Normal To Oily Skin |
Package Description | 5 mL in 1 TUBE (43596-0006-1) |
Product NDC | 43596-0006 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ENSULIZOLE, HOMOSALATE, OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120328 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Ventura Corporation, LTD |
Substance Name | ENSULIZOLE; HOMOSALATE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE |
Strength Number | 1.5; 1; 7.5; 4.5; 1.17 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |