DR. C. TUNA LUMI RADIANCE BRIGHTENING CREAM- octocrylene, octinoxate, avobenzone cream

Dr. C. Tuna Lumi Radiance Brightening Cream by

Drug Labeling and Warnings

Dr. C. Tuna Lumi Radiance Brightening Cream by is a Otc medication manufactured, distributed, or labeled by Farmasi US LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts:

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?

info@farmasius.com (833) 432-7627 Monday – Friday (9 a.m – 9 p.m. EST)

Package Labeling:

INGREDIENTS AND APPEARANCE

DR. C. TUNA LUMI RADIANCE BRIGHTENING CREAM 
octocrylene, octinoxate, avobenzone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74690-013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	55 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	60 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
STEARIC ACID (UNII: 4ELV7Z65AP)
MINERAL OIL (UNII: T5L8T28FGP)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
GLYCERIN (UNII: PDC6A3C0OX)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
CETEARETH-12 (UNII: 7V4MR24V5P)
CETYL PALMITATE (UNII: 5ZA2S6B08X)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
DIMETHICONE (UNII: 92RU3N3Y1O)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
NIACINAMIDE (UNII: 25X51I8RD4)
TROLAMINE (UNII: 9O3K93S3TK)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74690-013-01	1 in 1 BOX	07/25/2021
1		50 mL in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	07/25/2021

Labeler - Farmasi US LLC (113303351)