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Clarins Sunscreen High Protection SPF 30
Clarins Sunscreen High Protection SPF 30 - 58668-4411-1 - (OCTOCRYLENE, OCTINOXATE, TITANIUM DIOXIDE, ENSULIZOLE)
Drug Information of Clarins Sunscreen High Protection SPF 30
| Product NDC: | 58668-4411 |
| Proprietary Name: | Clarins Sunscreen High Protection SPF 30 |
| Non Proprietary Name: | OCTOCRYLENE, OCTINOXATE, TITANIUM DIOXIDE, ENSULIZOLE |
| Active Ingredient(s): | 3; 7.5; 9; 3.24 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTOCRYLENE, OCTINOXATE, TITANIUM DIOXIDE, ENSULIZOLE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clarins Sunscreen High Protection SPF 30
| Product NDC: | 58668-4411 |
| Labeler Name: | Laboratoires Clarins S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100805 |
Package Information of Clarins Sunscreen High Protection SPF 30
| Package NDC: | 58668-4411-1 |
| Package Description: | 1 TUBE in 1 PACKAGE (58668-4411-1) > 125 mL in 1 TUBE |
NDC Information of Clarins Sunscreen High Protection SPF 30
| NDC Code | 58668-4411-1 |
| Proprietary Name | Clarins Sunscreen High Protection SPF 30 |
| Package Description | 1 TUBE in 1 PACKAGE (58668-4411-1) > 125 mL in 1 TUBE |
| Product NDC | 58668-4411 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTOCRYLENE, OCTINOXATE, TITANIUM DIOXIDE, ENSULIZOLE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100805 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laboratoires Clarins S.A. |
| Substance Name | ENSULIZOLE; OCTINOXATE; OCTOCRYLENE; TITANIUM DIOXIDE |
| Strength Number | 3; 7.5; 9; 3.24 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
