Home > National Drug Code (NDC) > Rimmel London

Rimmel London - 59351-0314-1 - (Octinoxate, Octisalate)

Alphabetical Index


Drug Information of Rimmel London

Product NDC: 59351-0314
Proprietary Name: Rimmel London
Non Proprietary Name: Octinoxate, Octisalate
Active Ingredient(s): .012; .12    mL/6mL; mL/6mL & nbsp;   Octinoxate, Octisalate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Rimmel London

Product NDC: 59351-0314
Labeler Name: Lancaster S.A.M.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20101020

Package Information of Rimmel London

Package NDC: 59351-0314-1
Package Description: 6 mL in 1 TUBE (59351-0314-1)

NDC Information of Rimmel London

NDC Code 59351-0314-1
Proprietary Name Rimmel London
Package Description 6 mL in 1 TUBE (59351-0314-1)
Product NDC 59351-0314
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate, Octisalate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20101020
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Lancaster S.A.M.
Substance Name OCTINOXATE; OCTISALATE
Strength Number .012; .12
Strength Unit mL/6mL; mL/6mL
Pharmaceutical Classes

Complete Information of Rimmel London


General Information