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CLARINS UV PLUS HP Broad Spectrum SPF 40 Sunscreen Multi-Protection Tint DEEP
CLARINS UV PLUS HP Broad Spectrum SPF 40 Sunscreen Multi-Protection Tint DEEP - 58668-2921-1 - (TITANIUM DIOXIDE)
Drug Information of CLARINS UV PLUS HP Broad Spectrum SPF 40 Sunscreen Multi-Protection Tint DEEP
| Product NDC: | 58668-2921 |
| Proprietary Name: | CLARINS UV PLUS HP Broad Spectrum SPF 40 Sunscreen Multi-Protection Tint DEEP |
| Non Proprietary Name: | TITANIUM DIOXIDE |
| Active Ingredient(s): | 81 mg/mL & nbsp; TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CLARINS UV PLUS HP Broad Spectrum SPF 40 Sunscreen Multi-Protection Tint DEEP
| Product NDC: | 58668-2921 |
| Labeler Name: | Laboratoires Clarins S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121025 |
Package Information of CLARINS UV PLUS HP Broad Spectrum SPF 40 Sunscreen Multi-Protection Tint DEEP
| Package NDC: | 58668-2921-1 |
| Package Description: | 50 mL in 1 BOTTLE (58668-2921-1) |
NDC Information of CLARINS UV PLUS HP Broad Spectrum SPF 40 Sunscreen Multi-Protection Tint DEEP
| NDC Code | 58668-2921-1 |
| Proprietary Name | CLARINS UV PLUS HP Broad Spectrum SPF 40 Sunscreen Multi-Protection Tint DEEP |
| Package Description | 50 mL in 1 BOTTLE (58668-2921-1) |
| Product NDC | 58668-2921 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20121025 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Laboratoires Clarins S.A. |
| Substance Name | TITANIUM DIOXIDE |
| Strength Number | 81 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
