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MULTI PERFECTION SPECIAL EFFECTOR - 51346-046-01 - (OCTINOXATE, OCTISALATE)

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Drug Information of MULTI PERFECTION SPECIAL EFFECTOR

Product NDC: 51346-046
Proprietary Name: MULTI PERFECTION SPECIAL EFFECTOR
Non Proprietary Name: OCTINOXATE, OCTISALATE
Active Ingredient(s): 7.87; 4.2    g/105mL; g/105mL & nbsp;   OCTINOXATE, OCTISALATE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of MULTI PERFECTION SPECIAL EFFECTOR

Product NDC: 51346-046
Labeler Name: NATURE REPUBLIC CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120102

Package Information of MULTI PERFECTION SPECIAL EFFECTOR

Package NDC: 51346-046-01
Package Description: 105 mL in 1 CARTON (51346-046-01)

NDC Information of MULTI PERFECTION SPECIAL EFFECTOR

NDC Code 51346-046-01
Proprietary Name MULTI PERFECTION SPECIAL EFFECTOR
Package Description 105 mL in 1 CARTON (51346-046-01)
Product NDC 51346-046
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, OCTISALATE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120102
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name NATURE REPUBLIC CO., LTD.
Substance Name OCTINOXATE; OCTISALATE
Strength Number 7.87; 4.2
Strength Unit g/105mL; g/105mL
Pharmaceutical Classes

Complete Information of MULTI PERFECTION SPECIAL EFFECTOR


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