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Clarins UV Plus HP SPF 40 Day Screen High Protection
Clarins UV Plus HP SPF 40 Day Screen High Protection - 58668-2872-1 - (TITANIUM DIOXIDE)
Drug Information of Clarins UV Plus HP SPF 40 Day Screen High Protection
| Product NDC: | 58668-2872 |
| Proprietary Name: | Clarins UV Plus HP SPF 40 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): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clarins UV Plus HP SPF 40 Day Screen High Protection
| Product NDC: | 58668-2872 |
| Labeler Name: | Laboratoires Clarins S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100930 |
Package Information of Clarins UV Plus HP SPF 40 Day Screen High Protection
| Package NDC: | 58668-2872-1 |
| Package Description: | 1 BOTTLE in 1 PACKAGE (58668-2872-1) > 50 mL in 1 BOTTLE |
NDC Information of Clarins UV Plus HP SPF 40 Day Screen High Protection
| NDC Code | 58668-2872-1 |
| Proprietary Name | Clarins UV Plus HP SPF 40 Day Screen High Protection |
| Package Description | 1 BOTTLE in 1 PACKAGE (58668-2872-1) > 50 mL in 1 BOTTLE |
| Product NDC | 58668-2872 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100930 |
| 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 |
