| Product NDC: | 11410-839 |
| Proprietary Name: | Ice Elements |
| Non Proprietary Name: | Octinoxate, Octisalate, and Oxybenzone |
| Active Ingredient(s): | .075; .05; .03 mL/mL; mL/mL; mg/mL & nbsp; Octinoxate, Octisalate, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11410-839 |
| Labeler Name: | Guthy-Renker LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100224 |
| Package NDC: | 11410-839-11 |
| Package Description: | 30 mL in 1 TUBE (11410-839-11) |
| NDC Code | 11410-839-11 |
| Proprietary Name | Ice Elements |
| Package Description | 30 mL in 1 TUBE (11410-839-11) |
| Product NDC | 11410-839 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, and Oxybenzone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100224 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Guthy-Renker LLC |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | .075; .05; .03 |
| Strength Unit | mL/mL; mL/mL; mg/mL |
| Pharmaceutical Classes |