| Product NDC: | 76021-100 |
| Proprietary Name: | Life Extension Sun Protection SPF 30 |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
| Active Ingredient(s): | .65; 7.5; 3; 5 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76021-100 |
| Labeler Name: | LifeExtension Foundation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110210 |
| Package NDC: | 76021-100-06 |
| Package Description: | 178 mL in 1 BOTTLE (76021-100-06) |
| NDC Code | 76021-100-06 |
| Proprietary Name | Life Extension Sun Protection SPF 30 |
| Package Description | 178 mL in 1 BOTTLE (76021-100-06) |
| Product NDC | 76021-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20110210 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | LifeExtension Foundation |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | .65; 7.5; 3; 5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |