Home NDC 62839-2011 Sunright 50
Product NDC 62839-2011
11-digit product format 628392011
Labeler code 62839
Product ID 62839-2011_b43a24fc-7faa-4721-9f72-7fc5b4fd857c
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, and Octinoxate
Dosage form LOTION
Route TOPICAL
Labeler NSE Products, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-05-01
Substance AVOBENZONE; HOMOSALATE; OCTINOXATE
Active strength 30; 150; 50 mg/mL; mg/mL; mg/mL
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 Sunright 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL HOMOSALATE 150 mg/mL OCTINOXATE 50 mg/mL
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 4Y5P7MUD51 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 62839-2011-1 Sunright 50 100 mL in 1 TUBE LOTION 100 1
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 Sample Exclude flag Status 62839-2011-1 62839201101 100 mL in 1 TUBE (62839-2011-1) 100 ml 2021-05-01 No No Current