Product NDC: | 49967-445 |
Proprietary Name: | Kiehls Since 1851 Dermatologist Solutions Skin Tone Correcting and Beautifying BB Sunscreen |
Non Proprietary Name: | Homosalate, Octisalate, Octocrylene and Titanium dioxide |
Active Ingredient(s): | 100; 50; 50; 45 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Homosalate, Octisalate, Octocrylene and Titanium dioxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49967-445 |
Labeler Name: | L'Oreal USA Products Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130301 |
Package NDC: | 49967-445-01 |
Package Description: | 1 TUBE in 1 CARTON (49967-445-01) > 40 mL in 1 TUBE |
NDC Code | 49967-445-01 |
Proprietary Name | Kiehls Since 1851 Dermatologist Solutions Skin Tone Correcting and Beautifying BB Sunscreen |
Package Description | 1 TUBE in 1 CARTON (49967-445-01) > 40 mL in 1 TUBE |
Product NDC | 49967-445 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Homosalate, Octisalate, Octocrylene and Titanium dioxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130301 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | L'Oreal USA Products Inc |
Substance Name | HOMOSALATE; OCTISALATE; OCTOCRYLENE; TITANIUM DIOXIDE |
Strength Number | 100; 50; 50; 45 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |