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