NDC 51414-907

Sunscreen

Octocrylene ,homosalate,avobenzone,octisalate

Sunscreen is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Yuyao Jessie Commodity Co.,ltd.. The primary component is Homosalate; Octocrylene; Avobenzone; Octisalate.

Product ID51414-907_77220c16-6bd7-8780-e053-2991aa0ad2b3
NDC51414-907
Product TypeHuman Otc Drug
Proprietary NameSunscreen
Generic NameOctocrylene ,homosalate,avobenzone,octisalate
Dosage FormLotion
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 NameHOMOSALATE; OCTOCRYLENE; AVOBENZONE; OCTISALATE
Active Ingredient Strength10 g/100g; g/100g; g/100g; g/100g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 51414-907-01

5 g in 1 BOTTLE (51414-907-01)
Marketing Start Date2016-12-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51414-907-02 [51414090702]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-07 [51414090707]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-05 [51414090705]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-04 [51414090704]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-17 [51414090717]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-10 [51414090710]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-20 [51414090720]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-18 [51414090718]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-16 [51414090716]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-03 [51414090703]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-01 [51414090701]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-14 [51414090714]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-06 [51414090706]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-12 [51414090712]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-13 [51414090713]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-09 [51414090709]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-19 [51414090719]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-15 [51414090715]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-08 [51414090708]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

NDC 51414-907-11 [51414090711]

Sunscreen LOTION
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-11

Drug Details

Active Ingredients

IngredientStrength
HOMOSALATE10 g/100g

OpenFDA Data

SPL SET ID:77220c16-6bd6-8780-e053-2991aa0ad2b3
Manufacturer
UNII

NDC Crossover Matching brand name "Sunscreen" or generic name "Octocrylene ,homosalate,avobenzone,octisalate"

NDCBrand NameGeneric Name
0869-0055SunscreenAvobenzone, Homosalate, Octisalate, Octocrylene
0869-0059SunscreenSunscreen
0869-0109SunscreenAvobenzone, Homosalate, Octisalate, Octocrylene
0869-0727SunscreenAvobenzone, Homosalate, Octisalate, Oxybenzone
0869-0729SunscreenAvobenzone, Homosalate, Octisalate, Oxybenzone
0869-0730SunscreenAvobenzone, Homosalate, Octisalate, Oxybenzone
0869-0752SunscreenAvobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
0869-0787SunscreenAvobenzone, Homosalate, Octisalate, Oxybenzone
0869-0788SunscreenAvobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
0869-0789SunscreenAvobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
70412-210SunscreenSunscreen
70412-239SunscreenSunscreen
70306-5357sunscreensunscreen
70412-230SunscreenSunscreen
71011-004SunscreenSunscreen
72239-002SunscreenSunscreen
72239-001SunscreenSunscreen
0869-0790SunscreenSunscreen
19392-400sunscreensunscreen
19392-300sunscreensunscreen
30142-764SunscreenSunscreen
30142-714SunscreenSunscreen
30142-711SunscreenSunscreen
35192-008SunscreenSunscreen
51414-906SunscreenSunscreen
51414-905SUNSCREENSUNSCREEN
51414-907SunscreenSunscreen
52675-030SunScreenSunScreen
55319-788SunscreenSunscreen
55319-752SunscreenSunscreen
55319-787SunscreenSunscreen
55319-789SunscreenSunscreen
55319-790SunscreenSunscreen
55319-764SunscreenSunscreen
55550-102SunscreenSunscreen
55319-727SunscreenSunscreen
55910-788SunscreenSunscreen
55910-787SunscreenSunscreen
55910-789SunscreenSunscreen
55910-727SunscreenSunscreen
55910-764SunscreenSunscreen
61010-6103SunscreenSunscreen
62932-154SUNSCREENSUNSCREEN
62932-174SUNSCREENSUNSCREEN
62932-191SUNSCREENSUNSCREEN
62932-189SUNSCREENSUNSCREEN
62932-161SunscreenSunscreen
62932-165SunscreenSunscreen
62932-168SUNSCREENSUNSCREEN
62932-173SUNSCREENSUNSCREEN

Trademark Results [Sunscreen]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SUNSCREEN
SUNSCREEN
98196212 not registered Live/Pending
Unchained Labs, LLC
2023-09-25
SUNSCREEN
SUNSCREEN
98002932 not registered Live/Pending
So.Ai
2023-05-18
SUNSCREEN
SUNSCREEN
98002923 not registered Live/Pending
So.Ai
2023-05-18
SUNSCREEN
SUNSCREEN
97266768 not registered Live/Pending
ERL Clothing, LLC
2022-02-14
SUNSCREEN
SUNSCREEN
88145145 5865937 Live/Registered
Swinerton Incorporated
2018-10-05
SUNSCREEN
SUNSCREEN
87020645 not registered Dead/Abandoned
Sunscreen Display Technologies, LLC
2016-05-01
SUNSCREEN
SUNSCREEN
86891914 not registered Dead/Abandoned
IMAGN LLC
2016-01-29
SUNSCREEN
SUNSCREEN
86201962 4737576 Live/Registered
HEYCO PRODUCTS CORP.
2014-02-24
SUNSCREEN
SUNSCREEN
85051743 not registered Dead/Abandoned
U.S. Vision, Inc.
2010-06-01
SUNSCREEN
SUNSCREEN
79135388 4578067 Live/Registered
FAKRO Sp. z o.o.
2013-02-05
SUNSCREEN
SUNSCREEN
78549416 not registered Dead/Abandoned
Tree Introductions, Inc.
2005-01-18
SUNSCREEN
SUNSCREEN
76581251 3064741 Dead/Cancelled
Creative Flooring Systems, Inc.
2004-03-15

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.