Home NDC 75936-350 Glow Screen Body Broad Spectrum Sunscreen SPF 40
Product NDC 75936-350
11-digit product format 759360350
Labeler code 75936
Product ID 75936-350_47fbf731-a6d1-993f-e063-6294a90ad3f8
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form CREAM
Route TOPICAL
Labeler Supergoop, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-01-20
Substance HOMOSALATE; OCTISALATE; OCTOCRYLENE; AVOBENZONE
Active strength 7; 5; 10; 3 g/100mL; 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 Glow Screen Body Broad Spectrum Sunscreen SPF 40
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 7 g/100mL OCTISALATE 5 g/100mL OCTOCRYLENE 10 g/100mL AVOBENZONE 3 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 75936-350-01 Glow Screen Body Broad Spectrum Sunscreen SPF 40 100 mL in 1 TUBE CREAM 100 4 75936-350-02 Glow Screen Body Broad Spectrum Sunscreen SPF 40 10 mL in 1 TUBE CREAM 10 4 75936-350-03 Glow Screen Body Broad Spectrum Sunscreen SPF 40 15 mL in 1 TUBE CREAM 15 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75936-350 GLOW SCREEN BODY BROAD SPECTRUM SUNSCREEN SPF 40 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) CREAM [SUPERGOOP, LLC] 3 Current NDC, Legacy NDC, 3 package rows 20241207_b9590938-417d-617a-e053-2995a90a7496.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 45 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 75936-350-01 75936035001 100 mL in 1 TUBE (75936-350-01) 100 ml 2021-01-20 0000-00-00 No No Current 75936-350-02 75936035002 10 mL in 1 TUBE (75936-350-02) 10 ml 2021-01-20 0000-00-00 No No Current 75936-350-03 75936035003 15 mL in 1 TUBE (75936-350-03) 15 ml 2021-01-20 0000-00-00 No No Current