Home > National Drug Code (NDC) > TRUFFLE EX SUN

TRUFFLE EX SUN - 51346-002-01 - (OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE)

Alphabetical Index


Drug Information of TRUFFLE EX SUN

Product NDC: 51346-002
Proprietary Name: TRUFFLE EX SUN
Non Proprietary Name: OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE
Active Ingredient(s): 3.75; 2.5; 1.25; 2.4    g/50mL; g/50mL; g/50mL; g/50mL & nbsp;   OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of TRUFFLE EX SUN

Product NDC: 51346-002
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 TRUFFLE EX SUN

Package NDC: 51346-002-01
Package Description: 50 mL in 1 CARTON (51346-002-01)

NDC Information of TRUFFLE EX SUN

NDC Code 51346-002-01
Proprietary Name TRUFFLE EX SUN
Package Description 50 mL in 1 CARTON (51346-002-01)
Product NDC 51346-002
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE
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; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number 3.75; 2.5; 1.25; 2.4
Strength Unit g/50mL; g/50mL; g/50mL; g/50mL
Pharmaceutical Classes

Complete Information of TRUFFLE EX SUN


General Information