Home NDC 74690-013 Dr. C. Tuna Lumi Radiance Brightening Cream
Product NDC 74690-013
11-digit product format 746900013
Labeler code 74690
Product ID 74690-013_09735b00-e28e-ab1f-e063-6294a90a81ea
Type HUMAN OTC DRUG
Nonproprietary name OCTOCRYLENE, OCTINOXATE, AVOBENZONE
Dosage form CREAM
Route TOPICAL
Labeler Farmasi US LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-07-25
Substance OCTOCRYLENE; OCTINOXATE; AVOBENZONE
Active strength 55; 60; 20 mg/mL; mg/mL; mg/mL
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 Dr. C. Tuna Lumi Radiance Brightening Cream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 55 mg/mL OCTINOXATE 60 mg/mL AVOBENZONE 20 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5A68WGF6WM Internal UNII lookup 4Y5P7MUD51 Internal UNII lookup G63QQF2NOX 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 74690-013-01 Dr. C. Tuna Lumi Radiance Brightening Cream 50 mL in 1 JAR CREAM 50 2 74690-013-01 Dr. C. Tuna Lumi Radiance Brightening Cream 1 in 1 BOX CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 74690-013 DR. C. TUNA LUMI RADIANCE BRIGHTENING CREAM (OCTOCRYLENE, OCTINOXATE, AVOBENZONE) CREAM [FARMASI US LLC] 2 Current NDC, Legacy NDC, 2 package rows 20231106_b55790f7-20f2-404e-9a0e-5e76c383bf75.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 153 of 346 · 6,912 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 74690-013-01 74690001301 1 JAR in 1 BOX (74690-013-01) / 50 mL in 1 JAR 1 jar 2021-07-25 0000-00-00 No No Current