Home NDC 75936-210 Everyday Sunscreen with Sunflower Extract Broad Spectrum SPF 30
Product NDC 75936-210
11-digit product format 759360210
Labeler code 75936
Product ID 75936-210_47f8af2a-7636-44e9-e063-6294a90aa28c
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate
Dosage form CREAM
Route TOPICAL
Labeler Supergoop, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-02-12
Substance AVOBENZONE; HOMOSALATE; OCTISALATE
Active strength 3; 10; 5 g/100mL; g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Everyday Sunscreen with Sunflower Extract Broad Spectrum SPF 30
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 3 g/100mL HOMOSALATE 10 g/100mL OCTISALATE 5 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup V06SV4M95S Internal UNII lookup 4X49Y0596W Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 75936-210-01 Everyday Sunscreen with Sunflower Extract Broad Spectrum SPF 30 71 mL in 1 BOTTLE CREAM 71 7 75936-210-03 Everyday Sunscreen with Sunflower Extract Broad Spectrum SPF 30 162 mL in 1 BOTTLE CREAM 162 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75936-210 EVERYDAY SUNSCREEN WITH SUNFLOWER EXTRACT BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE) CREAM [SUPERGOOP, LLC] 6 Current NDC, Legacy NDC, 2 package rows 20241207_81b9fda2-bd55-1b90-e053-2991aa0a765a.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 75936-210-01 75936021001 71 mL in 1 BOTTLE (75936-210-01) 71 ml 2019-02-12 0000-00-00 No No Current 75936-210-02 75936021002 222 mL in 1 BOTTLE (75936-210-02) 222 ml 2019-02-12 0000-00-00 No No Current 75936-210-03 75936021003 162 mL in 1 BOTTLE (75936-210-03) 162 ml 2019-02-12 0000-00-00 No No Current