| Product NDC: | 49967-631 |
| Proprietary Name: | Kiehls Since 1851 Activated Sun Protector for Face Broad Spectrum SPF 50 Sunscreen |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Octocrylene and Oxybenzone |
| Active Ingredient(s): | 30; 150; 50; 50; 60 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Homosalate, Octisalate, Octocrylene and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49967-631 |
| 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: | 20130601 |
| Package NDC: | 49967-631-01 |
| Package Description: | 100 mL in 1 BOTTLE, PLASTIC (49967-631-01) |
| NDC Code | 49967-631-01 |
| Proprietary Name | Kiehls Since 1851 Activated Sun Protector for Face Broad Spectrum SPF 50 Sunscreen |
| Package Description | 100 mL in 1 BOTTLE, PLASTIC (49967-631-01) |
| Product NDC | 49967-631 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 30; 150; 50; 50; 60 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |