Active Ingredient
Octocrylene 5.5%
Ethylhexyl Methoxycinnamate 6%
Butyl Methoxydibenzoylmethane 2%
Dr. C. Tuna Lumi Radiance Brightening Cream 22 Spf Kit
FDA Label NDC 74690-023
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Farmasi Us Llc for the product Dr. C. Tuna Lumi Radiance Brightening Cream 22 Spf (NDC 74690-023). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, keep out of reach of children., directions, inactive ingredients:, package labeling:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Sunscreen
Use
Helps maintain bright skins and balance uneven skin tone with regular use.
Warnings
For external use only. Avoid contact with eyes. If contact occurs rinse thoroughly with water.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Recommended to use twice a day.
Inactive Ingredients:
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:
Label2 (Label2)
* Please review the disclaimer below.
