NDC 62296-7778

SPF 30 Sheer sunscreen face Ulta

Avobenzone 2.00% Homosalate 15.00% Octinoxate 7.50% Octisalate 5.00%

SPF 30 Sheer sunscreen face Ulta is a Topical Stick in the Human Otc Drug category. It is labeled and distributed by Ulta. The primary component is Avobenzone; Homosalate; Octinoxate; Octisalate.

Product ID62296-7778_5e448a1b-c28b-4ff0-9154-614ee50d5e52
NDC62296-7778
Product TypeHuman Otc Drug
Proprietary NameSPF 30 Sheer sunscreen face Ulta
Generic NameAvobenzone 2.00% Homosalate 15.00% Octinoxate 7.50% Octisalate 5.00%
Dosage FormStick
Route of AdministrationTOPICAL
Marketing Start Date2016-01-27
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart352
Labeler NameUlta
Substance NameAVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE
Active Ingredient Strength2 g/100g; g/100g; g/100g; g/100g
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 62296-7778-1

4.2 g in 1 TUBE (62296-7778-1)
Marketing Start Date2016-01-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62296-7778-1 [62296777801]

SPF 30 Sheer sunscreen face Ulta STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
AVOBENZONE2 g/100g

OpenFDA Data

SPL SET ID:c02b4223-a533-4fd9-b16b-4590cf325204
Manufacturer
UNII

NDC Crossover Matching brand name "SPF 30 Sheer sunscreen face Ulta" or generic name "Avobenzone 2.00% Homosalate 15.00% Octinoxate 7.50% Octisalate 5.00%"

NDCBrand NameGeneric Name
47124-447Sheer Sunscreen SPF 30Avobenzone 2.00% Homosalate 15.00% Octinoxate 7.50% Octisalate 5.00%
62296-7778SPF 30 Sheer sunscreen faceAvobenzone 2.00% Homosalate 15.00% Octinoxate 7.50% Octisalate 5.00%

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