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MANGO BEBE LIP ESSENCE - 51346-028-01 - (OCTINOXATE, OCTISALATE)

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Drug Information of MANGO BEBE LIP ESSENCE

Product NDC: 51346-028
Proprietary Name: MANGO BEBE LIP ESSENCE
Non Proprietary Name: OCTINOXATE, OCTISALATE
Active Ingredient(s): .6; .3    g/10mL; g/10mL & nbsp;   OCTINOXATE, OCTISALATE
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of MANGO BEBE LIP ESSENCE

Product NDC: 51346-028
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 MANGO BEBE LIP ESSENCE

Package NDC: 51346-028-01
Package Description: 10 mL in 1 CARTON (51346-028-01)

NDC Information of MANGO BEBE LIP ESSENCE

NDC Code 51346-028-01
Proprietary Name MANGO BEBE LIP ESSENCE
Package Description 10 mL in 1 CARTON (51346-028-01)
Product NDC 51346-028
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, OCTISALATE
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20120301
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name NATURE REPUBLIC CO., LTD.
Substance Name OCTINOXATE; OCTISALATE
Strength Number .6; .3
Strength Unit g/10mL; g/10mL
Pharmaceutical Classes

Complete Information of MANGO BEBE LIP ESSENCE


General Information