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Jurlique Sun Sunscreen SPF 30
Jurlique Sun Sunscreen SPF 30 - 68105-005-04 - (Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide)
Drug Information of Jurlique Sun Sunscreen SPF 30
| Product NDC: | 68105-005 |
| Proprietary Name: | Jurlique Sun Sunscreen SPF 30 |
| Non Proprietary Name: | Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide |
| Active Ingredient(s): | 75; 20; 50; 21 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM, AUGMENTED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Jurlique Sun Sunscreen SPF 30
| Product NDC: | 68105-005 |
| Labeler Name: | Jurlique International Pty. Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130101 |
Package Information of Jurlique Sun Sunscreen SPF 30
| Package NDC: | 68105-005-04 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (68105-005-04) > 30 mL in 1 BOTTLE, PUMP (68105-005-02) |
NDC Information of Jurlique Sun Sunscreen SPF 30
| NDC Code | 68105-005-04 |
| Proprietary Name | Jurlique Sun Sunscreen SPF 30 |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (68105-005-04) > 30 mL in 1 BOTTLE, PUMP (68105-005-02) |
| Product NDC | 68105-005 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide |
| Dosage Form Name | CREAM, AUGMENTED |
| Route Name | TOPICAL |
| Start Marketing Date | 20130101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Jurlique International Pty. Ltd. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 75; 20; 50; 21 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
