DR. C. TUNA RESURFACE ESSENTIAL DAY CREAM- homosalate, octinoxate, octocrylene, avobenzone cream

Dr. C. Tuna Resurface Essential Day Cream by

Drug Labeling and Warnings

Dr. C. Tuna Resurface Essential Day 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:

Homosalate 7% Ethylhexyl Methoxycinnamate 5% Octocrylene 5% Butyl Methoxydibenzoylmethane 2%

Purpose

Sunscreen

Use:

Helps to moisturize and protect the skin from sun damage.

Warnings:

For external use only.

Do not use

on damaged or broken skin.

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask doctor if

skin irritation develops when using this product.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

Directions: Use daily, every morning 15 minutes before sun exposure. Take enough amounts with the enclosed spatula on your hands; gently apply on clean face and neck.

Inactive Ingredients:

Water/Aqua, Cetyl Alcohol, Dicaprylyl Carbonate, Caprylic/Capric Triglyceride, Cichorium Intybus Leaf Extract, Hexylene Glycol, Caprylyl Glycol, Glyceryl Stearate SE, Phenoxyethanol, Cetyl Palmitate, Hexyldecanol, Hexyldecyl Laurate, Sodium Stearoyl Glutamate, Glycerin, Sodium Polyacrylate, Helianthus Annuus Seed Oil, Chlorella Vulgaris Extract, Rosmarinus Officinalis Leaf Extract, Niacinamide, Polymethylsilsesquioxane, Disodium EDTA, Xanthan Gum, Ethylhexylglycerin.

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 RESURFACE ESSENTIAL DAY CREAM 
homosalate, octinoxate, octocrylene, avobenzone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74690-016
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	70 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	50 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)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CHICORY LEAF (UNII: WBQ249COFR)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CETYL PALMITATE (UNII: 5ZA2S6B08X)
HEXYLDECANOL (UNII: 151Z7P1317)
HEXYLDECYL LAURATE (UNII: 0V595C1P6M)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
GLYCERIN (UNII: PDC6A3C0OX)
SUNFLOWER OIL (UNII: 3W1JG795YI)
CHLORELLA VULGARIS (UNII: RYQ4R60M02)
ROSEMARY (UNII: IJ67X351P9)
NIACINAMIDE (UNII: 25X51I8RD4)
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
XANTHAN GUM (UNII: TTV12P4NEE)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74690-016-01	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)