| 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 |