Home > National Drug Code (NDC) > 6 CREME 410 TEINTEE

6 CREME 410 TEINTEE - 51191-2013-1 - (OCTINOXATE)

Alphabetical Index


Drug Information of 6 CREME 410 TEINTEE

Product NDC: 51191-2013
Proprietary Name: 6 CREME 410 TEINTEE
Non Proprietary Name: OCTINOXATE
Active Ingredient(s): 5    g/100g & nbsp;   OCTINOXATE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of 6 CREME 410 TEINTEE

Product NDC: 51191-2013
Labeler Name: MULTALER & CIE S.A.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110215

Package Information of 6 CREME 410 TEINTEE

Package NDC: 51191-2013-1
Package Description: 50 g in 1 TUBE (51191-2013-1)

NDC Information of 6 CREME 410 TEINTEE

NDC Code 51191-2013-1
Proprietary Name 6 CREME 410 TEINTEE
Package Description 50 g in 1 TUBE (51191-2013-1)
Product NDC 51191-2013
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110215
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name MULTALER & CIE S.A.
Substance Name OCTINOXATE
Strength Number 5
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of 6 CREME 410 TEINTEE


General Information