| Product NDC: | 46007-202 |
| Proprietary Name: | AGE DEFYING MOISTURIZER |
| Non Proprietary Name: | AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE |
| Active Ingredient(s): | 2; 7.5; 5; 6 g/100mL; g/100mL; g/100mL; g/100mL & nbsp; AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 46007-202 |
| Labeler Name: | Skin Authority LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120419 |
| Package NDC: | 46007-202-12 |
| Package Description: | 50 mL in 1 BOTTLE (46007-202-12) |
| NDC Code | 46007-202-12 |
| Proprietary Name | AGE DEFYING MOISTURIZER |
| Package Description | 50 mL in 1 BOTTLE (46007-202-12) |
| Product NDC | 46007-202 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120419 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Skin Authority LLC |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 2; 7.5; 5; 6 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |