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THE FIRST SUN - 51346-001-01 - (OCTINOXATE, ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE)

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Drug Information of THE FIRST SUN

Product NDC: 51346-001
Proprietary Name: THE FIRST SUN
Non Proprietary Name: OCTINOXATE, ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE
Active Ingredient(s): 3; 2; 1; 2.61    g/40mL; g/40mL; g/40mL; g/40mL & nbsp;   OCTINOXATE, ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of THE FIRST SUN

Product NDC: 51346-001
Labeler Name: NATURE REPUBLIC CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120301

Package Information of THE FIRST SUN

Package NDC: 51346-001-01
Package Description: 40 mL in 1 CARTON (51346-001-01)

NDC Information of THE FIRST SUN

NDC Code 51346-001-01
Proprietary Name THE FIRST SUN
Package Description 40 mL in 1 CARTON (51346-001-01)
Product NDC 51346-001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20120301
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name NATURE REPUBLIC CO., LTD.
Substance Name OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number 3; 2; 1; 2.61
Strength Unit g/40mL; g/40mL; g/40mL; g/40mL
Pharmaceutical Classes

Complete Information of THE FIRST SUN


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