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Luminous Shield - 63730-220-01 - (Ensulizole, Octinoxate, Octocreylene, Oxybensone, Titanium Dioxide)

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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

Complete Information of Luminous Shield


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