| 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 |