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 |