Home NDC 75936-151 Hand Screen Broad Spectrum Sunscreen SPF 40
Product NDC 75936-151
11-digit product format 759360151
Labeler code 75936
Product ID 75936-151_47f864fd-a285-bc1d-e063-6294a90aa32d
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Octisalate, Octocrylene
Dosage form LOTION
Route TOPICAL
Labeler Supergoop, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-11-12
Substance OCTISALATE; AVOBENZONE; OCTOCRYLENE
Active strength 5; 3; 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 Hand Screen Broad Spectrum Sunscreen SPF 40
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 5 g/100mL AVOBENZONE 3 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 4X49Y0596W Internal UNII lookup G63QQF2NOX 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 75936-151-01 Hand Screen Broad Spectrum Sunscreen SPF 40 4 mL in 1 BOTTLE LOTION 4 8 75936-151-02 Hand Screen Broad Spectrum Sunscreen SPF 40 30 mL in 1 BOTTLE LOTION 30 8 75936-151-03 Hand Screen Broad Spectrum Sunscreen SPF 40 200 mL in 1 BOTTLE LOTION 200 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75936-151 HAND SCREEN BROAD SPECTRUM SUNSCREEN SPF 40 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) LOTION [SUPERGOOP, LLC] 7 Current NDC, Legacy NDC, 3 package rows 20241207_972ebab9-3f2f-6716-e053-2a95a90a5c75.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 109 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 75936-151-01 75936015101 4 mL in 1 BOTTLE (75936-151-01) 4 ml 2019-11-12 0000-00-00 No No Current 75936-151-02 75936015102 30 mL in 1 BOTTLE (75936-151-02) 30 ml 2019-11-12 0000-00-00 No No Current 75936-151-03 75936015103 200 mL in 1 BOTTLE (75936-151-03) 200 ml 2019-11-12 0000-00-00 No No Current