Product NDC: | 37205-722 |
Proprietary Name: | Leader |
Non Proprietary Name: | Octinoxate, Oxybenzone |
Active Ingredient(s): | 16.6; 4.15 mg/mL; mg/mL & nbsp; Octinoxate, Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37205-722 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120115 |
Package NDC: | 37205-722-30 |
Package Description: | 177 mL in 1 CAN (37205-722-30) |
NDC Code | 37205-722-30 |
Proprietary Name | Leader |
Package Description | 177 mL in 1 CAN (37205-722-30) |
Product NDC | 37205-722 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Oxybenzone |
Dosage Form Name | AEROSOL, SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20120115 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Cardinal Health |
Substance Name | OCTINOXATE; OXYBENZONE |
Strength Number | 16.6; 4.15 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |