Dr. C. Tuna Lumi Radiance Brightening Cream
FDA Label NDC 74690-003
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 (NDC 74690-003). 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 ingredients, purpose, use, warnings, directions, inactive ingredients, questions or comments?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Octocrylene 5.5%
Ethylhexyl Methoxycinnamate 6%
Butyl Methoxydibenzoylmethane 2%
Purpose
Sunscreen
Use
Helps to maintain skin brightness and balance uneven skin tone in regular use.
Warnings
For external use only. Avoid contact with eyes. If contact occurs rinse thoroughly with water.
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 Pamitate, Glyceryl Stearate, Butylene Glycol, Silica, Ammonium Polyacrylate, Hydrolyzed Algae Extract, Pancratium Maritimum Extract, Dimethicone, Phenoxyethanol, Fragrance / Parfum, Niacinamide, Triethanolamine, Ethylhexylglycerin, Tocopheryl Acetate.
Questions Or Comments?
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Package Labeling
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