Product NDC: | 11410-541 |
Proprietary Name: | Principal Secret |
Non Proprietary Name: | Octinoxate and Octisalate |
Active Ingredient(s): | 7.5; 1 mg/.1g; mg/.1g & nbsp; Octinoxate and Octisalate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11410-541 |
Labeler Name: | Guthy-Renker LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20020510 |
Package NDC: | 11410-541-34 |
Package Description: | 57 g in 1 JAR (11410-541-34) |
NDC Code | 11410-541-34 |
Proprietary Name | Principal Secret |
Package Description | 57 g in 1 JAR (11410-541-34) |
Product NDC | 11410-541 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate and Octisalate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20020510 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Guthy-Renker LLC |
Substance Name | OCTINOXATE; OCTISALATE |
Strength Number | 7.5; 1 |
Strength Unit | mg/.1g; mg/.1g |
Pharmaceutical Classes |