TRACELESS - 59158-731-01 - (OCTINOXATE)

Alphabetical Index


Drug Information of TRACELESS

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)

Labeler Information of TRACELESS

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 Information of TRACELESS

Package NDC: 59158-731-01
Package Description: 1 TUBE in 1 CARTON (59158-731-01) > 30 mL in 1 TUBE (59158-731-02)

NDC Information of TRACELESS

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

Complete Information of TRACELESS


General Information