| 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 |