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UV LOCK FLOWER SUN - 51346-211-01 - (OCTINOXATE, Titanium Dioxide, OCTISALATE)

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Drug Information of UV LOCK FLOWER SUN

Product NDC: 51346-211
Proprietary Name: UV LOCK FLOWER SUN
Non Proprietary Name: OCTINOXATE, Titanium Dioxide, OCTISALATE
Active Ingredient(s): 2.21; 1.47; 2.18    mg/150mL; mg/150mL; mg/150mL & nbsp;   OCTINOXATE, Titanium Dioxide, OCTISALATE
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of UV LOCK FLOWER SUN

Product NDC: 51346-211
Labeler Name: NATURE REPUBLIC CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130201

Package Information of UV LOCK FLOWER SUN

Package NDC: 51346-211-01
Package Description: 150 mL in 1 CARTON (51346-211-01)

NDC Information of UV LOCK FLOWER SUN

NDC Code 51346-211-01
Proprietary Name UV LOCK FLOWER SUN
Package Description 150 mL in 1 CARTON (51346-211-01)
Product NDC 51346-211
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, Titanium Dioxide, OCTISALATE
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20130201
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name NATURE REPUBLIC CO., LTD.
Substance Name OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE
Strength Number 2.21; 1.47; 2.18
Strength Unit mg/150mL; mg/150mL; mg/150mL
Pharmaceutical Classes

Complete Information of UV LOCK FLOWER SUN


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