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SUPER ORIGIN CC - 51346-217-01 - (TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, ZINC OXIDE)

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Drug Information of SUPER ORIGIN CC

Product NDC: 51346-217
Proprietary Name: SUPER ORIGIN CC
Non Proprietary Name: TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, ZINC OXIDE
Active Ingredient(s): 2.7; .9; 2.86; .86    g/45g; g/45g; g/45g; g/45g & nbsp;   TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of SUPER ORIGIN CC

Product NDC: 51346-217
Labeler Name: NATURE REPUBLIC CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130201

Package Information of SUPER ORIGIN CC

Package NDC: 51346-217-01
Package Description: 45 g in 1 CARTON (51346-217-01)

NDC Information of SUPER ORIGIN CC

NDC Code 51346-217-01
Proprietary Name SUPER ORIGIN CC
Package Description 45 g in 1 CARTON (51346-217-01)
Product NDC 51346-217
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, ZINC OXIDE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20130201
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name NATURE REPUBLIC CO., LTD.
Substance Name OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number 2.7; .9; 2.86; .86
Strength Unit g/45g; g/45g; g/45g; g/45g
Pharmaceutical Classes

Complete Information of SUPER ORIGIN CC


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