Dr. C. Tuna Lumi Radiance Brightening

Product NDC
74690-003
11-digit product format
746900003
Labeler code
74690
Product ID
74690-003_47f54023-5acc-8026-e063-6294a90a2b97
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
2020-01-08
Substance
AVOBENZONE; OCTINOXATE; OCTOCRYLENE
Active strength
20; 60; 55 mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Dr. C. Tuna Lumi Radiance Brightening
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE20 mg/mL
OCTINOXATE60 mg/mL
OCTOCRYLENE55 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, 4Y5P7MUD51, 5A68WGF6WM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74690-003-01Dr. C. Tuna Lumi Radiance Brightening1 in 1 BOXCREAM13
74690-003-01Dr. C. Tuna Lumi Radiance Brightening75 mL in 1 TUBECREAM753

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74690-003DR. C. TUNA LUMI RADIANCE BRIGHTENING (OCTOCRYLENE, OCTINOXATE, AVOBENZONE) CREAM [FARMASI US LLC]2Current NDC, Legacy NDC, 2 package rows20231213_adf5621b-7cf0-53b3-e053-2a95a90a8058.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
74690-003-01746900003011 TUBE in 1 BOX (74690-003-01) / 75 mL in 1 TUBE1 tube2020-01-080000-00-00NoNoCurrent