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

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Dr. C. Tuna Resurface Essential Day Cream

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:

Label4

DR. C. TUNA RESURFACE ESSENTIAL DAY CREAM 
homosalate, octinoxate, octocrylene, avobenzone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74690-016
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE70 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE50 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74690-016-011 in 1 BOX07/25/2021
150 mL in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02007/25/2021
Labeler - Farmasi US LLC (113303351)

Revised: 11/2023
Document Id: 097353b6-41d7-cea1-e063-6294a90aea19
Set id: b92ff1e9-9dc4-46cb-a99d-98ff15bffc79
Version: 2
Effective Time: 20231105
 
Farmasi US LLC