| Product NDC: | 10812-146 |
| Proprietary Name: | Neutrogena Age Defense Anti Oxidant Daily Moisturizer |
| Non Proprietary Name: | Homosalate, Octinoxate, Octisalate, and Oxybenzone |
| Active Ingredient(s): | 50; 75; 50; 20 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Homosalate, Octinoxate, Octisalate, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10812-146 |
| Labeler Name: | Neutrogena Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111031 |
| Package NDC: | 10812-146-10 |
| Package Description: | 1 TUBE in 1 CARTON (10812-146-10) > 50 mL in 1 TUBE |
| NDC Code | 10812-146-10 |
| Proprietary Name | Neutrogena Age Defense Anti Oxidant Daily Moisturizer |
| Package Description | 1 TUBE in 1 CARTON (10812-146-10) > 50 mL in 1 TUBE |
| Product NDC | 10812-146 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Homosalate, Octinoxate, Octisalate, and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20111031 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Neutrogena Corporation |
| Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 50; 75; 50; 20 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |