| Product NDC: | 11410-413 |
| Proprietary Name: | Natural Advantage SPF 15 All Day Moisture with AHAs |
| Non Proprietary Name: | octinoxate, oxybenzone, octisalate |
| Active Ingredient(s): | 75; 35; 40 uL/mL; uL/mL; uL/mL & nbsp; octinoxate, oxybenzone, octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11410-413 |
| Labeler Name: | Guthy-Renker LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091102 |
| Package NDC: | 11410-413-01 |
| Package Description: | 50 mL in 1 TUBE (11410-413-01) |
| NDC Code | 11410-413-01 |
| Proprietary Name | Natural Advantage SPF 15 All Day Moisture with AHAs |
| Package Description | 50 mL in 1 TUBE (11410-413-01) |
| Product NDC | 11410-413 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, oxybenzone, octisalate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20091102 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Guthy-Renker LLC |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 75; 35; 40 |
| Strength Unit | uL/mL; uL/mL; uL/mL |
| Pharmaceutical Classes |