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 |