Home
>
National Drug Code (NDC)
>
UV PLUS HP DAY SCREEN HIGH PROTECTION
UV PLUS HP DAY SCREEN HIGH PROTECTION - 58668-2832-1 - (TITANIUM DIOXIDE)
Drug Information of UV PLUS HP DAY SCREEN HIGH PROTECTION
| Product NDC: | 58668-2832 |
| Proprietary Name: | UV PLUS HP DAY SCREEN HIGH PROTECTION |
| Non Proprietary Name: | TITANIUM DIOXIDE |
| Active Ingredient(s): | 8.1 mL/100mL & nbsp; TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of UV PLUS HP DAY SCREEN HIGH PROTECTION
| Product NDC: | 58668-2832 |
| Labeler Name: | Laboratoires Clarins S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100319 |
Package Information of UV PLUS HP DAY SCREEN HIGH PROTECTION
| Package NDC: | 58668-2832-1 |
| Package Description: | 1 TUBE in 1 CARTON (58668-2832-1) > 50 mL in 1 TUBE |
NDC Information of UV PLUS HP DAY SCREEN HIGH PROTECTION
| NDC Code | 58668-2832-1 |
| Proprietary Name | UV PLUS HP DAY SCREEN HIGH PROTECTION |
| Package Description | 1 TUBE in 1 CARTON (58668-2832-1) > 50 mL in 1 TUBE |
| Product NDC | 58668-2832 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100319 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laboratoires Clarins S.A. |
| Substance Name | TITANIUM DIOXIDE |
| Strength Number | 8.1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
