Home NDC 75936-216 Glow Screen SPF 40
Product NDC 75936-216
11-digit product format 759360216
Labeler code 75936
Product ID 75936-216_47fc2146-2852-7663-e063-6394a90af7e9
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Octisalate, Octocylene
Dosage form CREAM
Route TOPICAL
Labeler Supergoop, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-01
Substance AVOBENZONE; OCTISALATE; OCTOCRYLENE
Active strength 3; 5; 10 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 SPF 40
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 3 g/100mL OCTISALATE 5 g/100mL OCTOCRYLENE 10 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 4X49Y0596W Internal UNII lookup 5A68WGF6WM Internal UNII lookup
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 75936-216-01 Glow Screen SPF 40 1.5 mL in 1 BOTTLE CREAM 1.5 8 75936-216-02 Glow Screen SPF 40 5 mL in 1 BOTTLE CREAM 5 8 75936-216-03 Glow Screen SPF 40 10 mL in 1 BOTTLE CREAM 10 8 75936-216-04 Glow Screen SPF 40 15 mL in 1 BOTTLE CREAM 15 8 75936-216-05 Glow Screen SPF 40 50 mL in 1 BOTTLE CREAM 50 8 75936-216-06 Glow Screen SPF 40 20 mL in 1 TUBE CREAM 20 8 75936-216-07 Glow Screen SPF 40 73.9 mL in 1 TUBE CREAM 73.9 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75936-216 GLOW SCREEN SPF 40 (AVOBENZONE, OCTISALATE, OCTOCYLENE) CREAM [SUPERGOOP, LLC] 7 Current NDC, Legacy NDC, 7 package rows 20241207_21569637-332a-461b-bf6c-33af6a83a155.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 75936-216-01 75936021601 1.5 mL in 1 BOTTLE (75936-216-01) 1.5 ml 2020-01-01 0000-00-00 No No Current 75936-216-02 75936021602 5 mL in 1 BOTTLE (75936-216-02) 5 ml 2020-01-01 0000-00-00 No No Current 75936-216-03 75936021603 10 mL in 1 BOTTLE (75936-216-03) 10 ml 2020-01-01 0000-00-00 No No Current 75936-216-04 75936021604 15 mL in 1 BOTTLE (75936-216-04) 15 ml 2020-01-01 0000-00-00 No No Current 75936-216-05 75936021605 50 mL in 1 BOTTLE (75936-216-05) 50 ml 2020-01-01 0000-00-00 No No Current 75936-216-06 75936021606 20 mL in 1 TUBE (75936-216-06) 20 ml 2021-05-18 0000-00-00 No No Current 75936-216-07 75936021607 73.9 mL in 1 TUBE (75936-216-07) 73.9 ml 2022-01-18 0000-00-00 No No Current