Product NDC: | 76450-050 |
Proprietary Name: | MOISTURISING SUN PROTECTION |
Non Proprietary Name: | OCTINOXATE |
Active Ingredient(s): | 1.5; 1; 1.5; 3 mL/50mL; mL/50mL; mL/50mL; mL/50mL & nbsp; OCTINOXATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76450-050 |
Labeler Name: | Mesoestetic, S.L. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120201 |
Package NDC: | 76450-050-01 |
Package Description: | 50 mL in 1 TUBE (76450-050-01) |
NDC Code | 76450-050-01 |
Proprietary Name | MOISTURISING SUN PROTECTION |
Package Description | 50 mL in 1 TUBE (76450-050-01) |
Product NDC | 76450-050 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Mesoestetic, S.L. |
Substance Name | AVOBENZONE; ENSULIZOLE; ENZACAMENE; OCTINOXATE |
Strength Number | 1.5; 1; 1.5; 3 |
Strength Unit | mL/50mL; mL/50mL; mL/50mL; mL/50mL |
Pharmaceutical Classes |