| Product NDC: | 11410-503 |
| Proprietary Name: | Daily Body Moisture Hydrating Complex SPF8 |
| Non Proprietary Name: | OCTINOXATE and OXYBENZONE |
| Active Ingredient(s): | 7.5; 1 mL/100mL; mL/100mL & nbsp; OCTINOXATE and OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11410-503 |
| Labeler Name: | Guthy-Renker LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050802 |
| Package NDC: | 11410-503-68 |
| Package Description: | 180 mL in 1 TUBE (11410-503-68) |
| NDC Code | 11410-503-68 |
| Proprietary Name | Daily Body Moisture Hydrating Complex SPF8 |
| Package Description | 180 mL in 1 TUBE (11410-503-68) |
| Product NDC | 11410-503 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20050802 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Guthy-Renker LLC |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 7.5; 1 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |