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 |