FDA.reportPublic FDA data

Dr. C. Tuna Lumi Radiance Brightening Cream 22 SPF

Manufacturer
Farmasi US LLC
Effective date
2023-11-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:59:09

Label at a glance#

ProductDr. C. Tuna Lumi Radiance Brightening Cream 22 SPF
Active ingredientOCTOCRYLENE, OCTINOXATE, AVOBENZONE
Label structure6 sections

Dosage and administration

Recommended to use twice a day.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Octocrylene 5.5%

Ethylhexyl Methoxycinnamate 6%

Butyl Methoxydibenzoylmethane 2%

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

USE

INDICATIONS & USAGE SECTION

Helps maintain bright skins and balance uneven skin tone with regular use.

WARNINGS

WARNINGS SECTION

For external use only. Avoid contact with eyes. If contact occurs rinse thoroughly with water.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Recommended to use twice a day.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Water/Aqua, Cetearyl Alcohol, Stearic Acid, Mineral Oil / Paraffinum Liquidum, Isopropyl Myristate, Glycerin, Titanium Dioxide, Ceteareth-20,  Ceteareth-12, Cetearyl Alcohol, Cetyl Palmitate, Glyceryl Stearate, Butylene Glycol, Silica, Ammonium Polyacrylate, Hydrolyzed Algae Extract, Pancratium Maritimum Extract, Dimethicone, Phenoxyethanol, Fragrance / Parfum, Niacinamide, Triethanolamine, Ethylhexylglycerin, Tocopheryl Acetate.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74690-023-00Dr. C. Tuna Lumi Radiance Brightening Cream 22 SPF1 in 1 KITKIT12
74690-024-00Dr. C. Tuna Lumi Radiance Brightening Cream 22 SPF2.5 mL in 1 PACKETCREAM2.5 mL60 mg in 1mL2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74690-023DR. C. TUNA LUMI RADIANCE BRIGHTENING CREAM 22 SPF (OCTOCRYLENE, OCTINOXATE, AVOBENZONE) KIT [FARMASI US LLC]2Current NDC, Legacy NDC, 2 package rows20231106_de493e30-d10e-9def-e053-2995a90ae49a.zip
74690-024DR. C. TUNA LUMI RADIANCE BRIGHTENING CREAM 22 SPF (OCTOCRYLENE, OCTINOXATE, AVOBENZONE) KIT [FARMASI US LLC]2Unmatched20231106_de493e30-d10e-9def-e053-2995a90ae49a.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74690-02374690-023-00
74690-02474690-024-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
STEARIC ACID4ELV7Z65APIACT
MINERAL OILT5L8T28FGPIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
GLYCERINPDC6A3C0OXIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
POLYOXYL 20 CETOSTEARYL ETHERYRC528SWUYIACT
CETEARETH-127V4MR24V5PIACT
CETYL PALMITATE5ZA2S6B08XIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
DIMETHICONE92RU3N3Y1OIACT
PHENOXYETHANOLHIE492ZZ3TIACT
NIACINAMIDE25X51I8RD4IACT
TROLAMINE9O3K93S3TKIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
OCTOCRYLENE5A68WGF6WMACTIB
OCTINOXATE4Y5P7MUD51ACTIB
AVOBENZONEG63QQF2NOXACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dr. C. Tuna Lumi Radiance Brightening Cream 22 SPFOCTOCRYLENE, OCTINOXATE, AVOBENZONEFarmasi US LLCde493e30-d10e-9def-e053-2995a90ae49a2023-11-05WarningsExact identifier
ndc (package): 74690-023-00
ndc (package): 74690-024-00
ndc (product): 74690-023
ndc11 (package): 74690002300
ndc11 (package): 74690002400
spl id: 09735b00-e2b5-ab1f-e063-6294a90a81ea
spl set id: de493e30-d10e-9def-e053-2995a90ae49a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.