Home NDC 84603-166 Basin Sun Stick
Product NDC 84603-166
11-digit product format 846030166
Labeler code 84603
Product ID 84603-166_3e77f39a-9a15-f581-e063-6394a90a0cae
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Octinoxate, Octisalate, Oxybenzone
Dosage form STICK
Route TOPICAL
Labeler Retail Concepts of Minnesota, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-01-25
Substance OCTINOXATE; OXYBENZONE; AVOBENZONE; OCTISALATE
Active strength 7.5; 4; 3; 5 g/100g; g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2026-12-31
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 Basin Sun Stick
Brand name suffix SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 7.5 g/100g OXYBENZONE 4 g/100g AVOBENZONE 3 g/100g OCTISALATE 5 g/100g
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84603-166-01 Basin Sun StickSPF 30 17 g in 1 TUBE STICK 17 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 84603-166-01 84603016601 17 g in 1 TUBE (84603-166-01) 17 g 2024-01-25 No No Current