| Product NDC: | 49967-707 |
| Proprietary Name: | Kiehls Since 1851 Dermatologist Solutions |
| Non Proprietary Name: | Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
| Active Ingredient(s): | 4.5; 22.5; 7.5; 7.5; 9 mL/150mL; mL/150mL; mL/150mL; mL/150mL; mL/150mL & nbsp; Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49967-707 |
| 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: | 20120601 |
| Package NDC: | 49967-707-01 |
| Package Description: | 150 mL in 1 BOTTLE, PLASTIC (49967-707-01) |
| NDC Code | 49967-707-01 |
| Proprietary Name | Kiehls Since 1851 Dermatologist Solutions |
| Package Description | 150 mL in 1 BOTTLE, PLASTIC (49967-707-01) |
| Product NDC | 49967-707 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 4.5; 22.5; 7.5; 7.5; 9 |
| Strength Unit | mL/150mL; mL/150mL; mL/150mL; mL/150mL; mL/150mL |
| Pharmaceutical Classes |