Dr. C. Tuna Lumi Radiance Brightening Cream
FDA Label NDC 74690-013
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 (NDC 74690-013). 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 drug facts:, active ingredient:, purpose, use:, warnings:, keep out of reach of children., directions:, other information:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient:
Octocrylene 5.5%
Ethylhexyl Methoxycinnamate 6%
Butyl Methoxydibenzoylmethane 2%
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.
Other Information:
Store at room temperature.
Inactive Ingredients:
Water/Aqua, Cetearyl Alcohol, Stearic Acid, Mineral Oil/Paraffinum Liquidum, Isopropyl Myristate, Glycerin, Titanium Dioxide, Ceteareth-20, Ceteareth-12, Cetyl Palmitate, Glyceryl Stearate, Butylene Glycol, Silica, Ammonium Polyacrylate, Hydrolyzed Algae Extract, Pancratium Maritimum Extract, Phyllanthus Emblica Extract, Dimethicone, Phenoxyethanol, Fragrance/Parfum, Niacinamide, Triethanolamine, Ethylhexylglycerin, Tocopheryl Acetate.
Questions Or Comments?
[email protected] (833) 432-7627 Monday – Friday (9 a.m – 9 p.m. EST)
Package Labeling:
Label (Label)
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