| Product NDC: | 59158-731 |
| Proprietary Name: | TRACELESS |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 2 mL/100mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59158-731 |
| Labeler Name: | PRESCRIPTIVES INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20010601 |
| Package NDC: | 59158-731-01 |
| Package Description: | 1 TUBE in 1 CARTON (59158-731-01) > 30 mL in 1 TUBE (59158-731-02) |
| NDC Code | 59158-731-01 |
| Proprietary Name | TRACELESS |
| Package Description | 1 TUBE in 1 CARTON (59158-731-01) > 30 mL in 1 TUBE (59158-731-02) |
| Product NDC | 59158-731 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20010601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | PRESCRIPTIVES INC. |
| Substance Name | OCTINOXATE |
| Strength Number | 2 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |