Home
>
National Drug Code (NDC)
>
ULTRAPROTECTION
ULTRAPROTECTION - 51191-2016-1 - (Octinoxate, Titanium dioxide)
Drug Information of ULTRAPROTECTION
| Product NDC: | 51191-2016 |
| Proprietary Name: | ULTRAPROTECTION |
| Non Proprietary Name: | Octinoxate, Titanium dioxide |
| Active Ingredient(s): | 7.5; 4.98 g/100g; g/100g & nbsp; Octinoxate, Titanium dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ULTRAPROTECTION
| Product NDC: | 51191-2016 |
| 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 ULTRAPROTECTION
| Package NDC: | 51191-2016-1 |
| Package Description: | 50 g in 1 TUBE (51191-2016-1) |
NDC Information of ULTRAPROTECTION
| NDC Code | 51191-2016-1 |
| Proprietary Name | ULTRAPROTECTION |
| Package Description | 50 g in 1 TUBE (51191-2016-1) |
| Product NDC | 51191-2016 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Titanium dioxide |
| 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; TITANIUM DIOXIDE |
| Strength Number | 7.5; 4.98 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
