Home NDC 74690-028 Dr. C. Tuna Sun Stick SPF 50
Product NDC 74690-028
11-digit product format 746900028
Labeler code 74690
Product ID 74690-028_49dc6085-b934-8106-e063-6394a90a63f9
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, OCTINOXATE, HOMOSALATE, OCTOCRYLENE
Dosage form STICK
Route TOPICAL
Labeler Farmasi US LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-08
Substance AVOBENZONE; OCTINOXATE; HOMOSALATE; OCTOCRYLENE
Active strength 29.5; 74.5; 73.4; 75 mg/g; mg/g; mg/g; mg/g
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 Dr. C. Tuna Sun Stick SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 29.5 mg/g OCTINOXATE 74.5 mg/g HOMOSALATE 73.4 mg/g OCTOCRYLENE 75 mg/g
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 74690-028-00 Dr. C. Tuna Sun Stick SPF 50 20 g in 1 BOTTLE, PLASTIC STICK 20 1 74690-028-00 Dr. C. Tuna Sun Stick SPF 50 1 in 1 CARTON STICK 1 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 Marketing start Sample Exclude flag Status 74690-028-00 74690002800 1 BOTTLE, PLASTIC in 1 CARTON (74690-028-00) / 20 g in 1 BOTTLE, PLASTIC 2026-01-08 No No Current