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Jurlique Purely Sun-Defying
Jurlique Purely Sun-Defying - 68105-004-01 - (ZINC OXIDE and TITANIUM DIOXIDE)
Drug Information of Jurlique Purely Sun-Defying
| Product NDC: | 68105-004 |
| Proprietary Name: | Jurlique Purely Sun-Defying |
| Non Proprietary Name: | ZINC OXIDE and TITANIUM DIOXIDE |
| Active Ingredient(s): | 2.1; 4.8 g/100g; g/100g & nbsp; ZINC OXIDE and TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM, AUGMENTED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Jurlique Purely Sun-Defying
| Product NDC: | 68105-004 |
| Labeler Name: | Jurlique International Pty. Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111101 |
Package Information of Jurlique Purely Sun-Defying
| Package NDC: | 68105-004-01 |
| Package Description: | 40 g in 1 TUBE (68105-004-01) |
NDC Information of Jurlique Purely Sun-Defying
| NDC Code | 68105-004-01 |
| Proprietary Name | Jurlique Purely Sun-Defying |
| Package Description | 40 g in 1 TUBE (68105-004-01) |
| Product NDC | 68105-004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE and TITANIUM DIOXIDE |
| Dosage Form Name | CREAM, AUGMENTED |
| Route Name | TOPICAL |
| Start Marketing Date | 20111101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Jurlique International Pty. Ltd. |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 2.1; 4.8 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
