Home > National Drug Code (NDC) > SPF15 sunscreen

SPF15 sunscreen - 51414-600-21 - (Octinoxate,oxybenzone,OCTISALATE)

Alphabetical Index


Drug Information of SPF15 sunscreen

Product NDC: 51414-600
Proprietary Name: SPF15 sunscreen
Non Proprietary Name: Octinoxate,oxybenzone,OCTISALATE
Active Ingredient(s): 4; 2; 4    g/100g; g/100g; g/100g & nbsp;   Octinoxate,oxybenzone,OCTISALATE
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of SPF15 sunscreen

Product NDC: 51414-600
Labeler Name: Yuyao Jessie Commodity Co.,Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120912

Package Information of SPF15 sunscreen

Package NDC: 51414-600-21
Package Description: 180 g in 1 PACKAGE (51414-600-21)

NDC Information of SPF15 sunscreen

NDC Code 51414-600-21
Proprietary Name SPF15 sunscreen
Package Description 180 g in 1 PACKAGE (51414-600-21)
Product NDC 51414-600
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate,oxybenzone,OCTISALATE
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20120912
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Yuyao Jessie Commodity Co.,Ltd.
Substance Name OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 4; 2; 4
Strength Unit g/100g; g/100g; g/100g
Pharmaceutical Classes

Complete Information of SPF15 sunscreen


General Information