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Luminous Shield
Luminous Shield - 63730-220-01 - (Ensulizole, Octinoxate, Octocreylene, Oxybensone, Titanium Dioxide)
Drug Information of Luminous Shield
| Product NDC: | 63730-220 |
| Proprietary Name: | Luminous Shield |
| Non Proprietary Name: | Ensulizole, Octinoxate, Octocreylene, Oxybensone, Titanium Dioxide |
| Active Ingredient(s): | 1.65; 4.9; 7.85; 2.47; 10.14 g/75mL; mL/75mL; mL/75mL; g/75mL; g/75mL & nbsp; Ensulizole, Octinoxate, Octocreylene, Oxybensone, Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Luminous Shield
| Product NDC: | 63730-220 |
| Labeler Name: | Natura Bisse International, S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100419 |
Package Information of Luminous Shield
| Package NDC: | 63730-220-01 |
| Package Description: | 75 mL in 1 TUBE (63730-220-01) |
NDC Information of Luminous Shield
| NDC Code | 63730-220-01 |
| Proprietary Name | Luminous Shield |
| Package Description | 75 mL in 1 TUBE (63730-220-01) |
| Product NDC | 63730-220 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ensulizole, Octinoxate, Octocreylene, Oxybensone, Titanium Dioxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100419 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Natura Bisse International, S.A. |
| Substance Name | ENSULIZOLE; OCTINOXATE; OCTOCRYLENE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 1.65; 4.9; 7.85; 2.47; 10.14 |
| Strength Unit | g/75mL; mL/75mL; mL/75mL; g/75mL; g/75mL |
| Pharmaceutical Classes |
