| Product NDC: | 11410-420 |
| Proprietary Name: | Jane Seymour Natural Advantage |
| Non Proprietary Name: | Octinoxate, Oxybenzone, and Octisalate |
| Active Ingredient(s): | .075; .035; .04 mL/mL; mL/mL; mg/mL & nbsp; Octinoxate, Oxybenzone, and Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11410-420 |
| Labeler Name: | Guthy-Renker LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080508 |
| Package NDC: | 11410-420-13 |
| Package Description: | 50 mL in 1 BOTTLE, DISPENSING (11410-420-13) |
| NDC Code | 11410-420-13 |
| Proprietary Name | Jane Seymour Natural Advantage |
| Package Description | 50 mL in 1 BOTTLE, DISPENSING (11410-420-13) |
| Product NDC | 11410-420 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Oxybenzone, and Octisalate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20080508 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Guthy-Renker LLC |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | .075; .035; .04 |
| Strength Unit | mL/mL; mL/mL; mg/mL |
| Pharmaceutical Classes |