Home NDC 84661-021 Sunplus SPF 50 Mist Sunscreen
Product NDC 84661-021
11-digit product format 846610021
Labeler code 84661
Product ID 84661-021_5df8bba2-240a-48a4-e063-6294a90a9132
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, OCTISALATE, OCTOCRYLENE
Dosage form LIQUID
Route TOPICAL
Labeler SUNPLUS SKIN CARE LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-09-29
Substance AVOBENZONE; OCTISALATE; OCTOCRYLENE
Active strength 30; 50; 100 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 Sunplus SPF 50 Mist Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 100 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 4X49Y0596W Internal UNII lookup 5A68WGF6WM Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 346 · 6,912 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84661-021-00 84661002100 89 mL in 1 CAN (84661-021-00) 89 ml 2026-09-29 No No Current