NDC 51414-600

SPF15 sunscreen

Octinoxate,oxybenzone,octisalate

SPF15 sunscreen is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Yuyao Jessie Commodity Co.,ltd.. The primary component is Octinoxate; Oxybenzone; Octisalate.

Product ID51414-600_6208ece6-7eb5-fd36-e053-2991aa0a603c
NDC51414-600
Product TypeHuman Otc Drug
Proprietary NameSPF15 sunscreen
Generic NameOctinoxate,oxybenzone,octisalate
Dosage FormSpray
Route of AdministrationTOPICAL
Marketing Start Date2012-09-12
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart352
Labeler NameYuyao Jessie Commodity Co.,Ltd.
Substance NameOCTINOXATE; OXYBENZONE; OCTISALATE
Active Ingredient Strength4 g/100g; g/100g; g/100g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 51414-600-01

5 g in 1 PACKAGE (51414-600-01)
Marketing Start Date2018-01-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51414-600-17 [51414060017]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-06 [51414060006]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-21 [51414060021]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-04 [51414060004]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-12 [51414060012]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-10 [51414060010]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-16 [51414060016]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-07 [51414060007]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-24 [51414060024]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-25 [51414060025]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-11 [51414060011]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-09 [51414060009]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-22 [51414060022]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-15 [51414060015]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-03 [51414060003]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-13 [51414060013]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-02 [51414060002]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-14 [51414060014]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-08 [51414060008]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-01 [51414060001]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-04

NDC 51414-600-20 [51414060020]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-19 [51414060019]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-18 [51414060018]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-23 [51414060023]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

NDC 51414-600-05 [51414060005]

SPF15 sunscreen SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01

Drug Details

Active Ingredients

IngredientStrength
OCTINOXATE4 g/100g

OpenFDA Data

SPL SET ID:8c9374ae-2522-4f98-99c3-90ce82657bb6
Manufacturer
UNII

NDC Crossover Matching brand name "SPF15 sunscreen" or generic name "Octinoxate,oxybenzone,octisalate"

NDCBrand NameGeneric Name
51414-600SPF15 sunscreenOctinoxate,oxybenzone,OCTISALATE
70412-212SPF15 SunscreenAVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE
51414-104SPF30 sunscreenOctinoxate,oxybenzone,OCTISALATE

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