Home > National Drug Code (NDC) > PLACENTA EX SUN BALM

PLACENTA EX SUN BALM - 51346-031-01 - (OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE)

Alphabetical Index


Drug Information of PLACENTA EX SUN BALM

Product NDC: 51346-031
Proprietary Name: PLACENTA EX SUN BALM
Non Proprietary Name: OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE
Active Ingredient(s): .84; .73; .59    g/12g; g/12g; g/12g & nbsp;   OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of PLACENTA EX SUN BALM

Product NDC: 51346-031
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 PLACENTA EX SUN BALM

Package NDC: 51346-031-01
Package Description: 12 g in 1 CARTON (51346-031-01)

NDC Information of PLACENTA EX SUN BALM

NDC Code 51346-031-01
Proprietary Name PLACENTA EX SUN BALM
Package Description 12 g in 1 CARTON (51346-031-01)
Product NDC 51346-031
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120301
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name NATURE REPUBLIC CO., LTD.
Substance Name OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number .84; .73; .59
Strength Unit g/12g; g/12g; g/12g
Pharmaceutical Classes

Complete Information of PLACENTA EX SUN BALM


General Information