SUNGBOON EDITOR DAILY INVISIBLE BLURRING SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene cream

Sungboon Editor Daily Invisible Blurring Sunscreen by

Drug Labeling and Warnings

Sungboon Editor Daily Invisible Blurring Sunscreen by is a Otc medication manufactured, distributed, or labeled by Olive International Inc., Rebom Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Homosalate 10%

Octocrylene 9.0%

Octisalate 4.9%

Avobenzone 2.9%

PURPOSE

Sunscreen

INDICATIONS & USAGE

Helps prevent sunburn
If used as directed with other sun protection measures (see Directions) decrease the risk of skin cancer and early skin aging caused by the sun

DOSAGE & ADMINISTRATION

Apply liberally 15 minutes before sun exposure

Children under 6 months or age: Ask a doctor.

Reapply at least every two hours
Use a water-resistant sunscreen if swimming or sweating
Sun protection measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF or 15 of higher and other sun protection measures including:

Limited time in the sun, especially from 10 am to 2 pm.

Wear long-sleeve shirts, pants, hats, and sunglasses

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 a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of the children.

If swallowed, get medical help or contact a poison control center right away.

INACTIVE INGREDIENT

Isododecane, Cyclopentasiloxane, Cyclohexasiloxane, Dimethicone/Bis-Isobutyl PPG-20 Crosspolymer, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Butyloctyl Salicylate, Polyglyceryl-4 Oleate, Water, C12-13 Pareth-9, Polyglyceryl-6 Oleate, Polyhydroxystearic Acid, Ethylhexylglycerin, Tocopherol, Tocopheryl Acetate, Helianthus Annuus (Sunflower) Seed Oil, Butylene Glycol, Glutathione, Niacinamide, Silica, Panthenol, 1,2-Hexanediol, Hippophae Rhamnoides Fruit Extract, Citrus Aurantium Dulcis (Orange) Fruit Extract, Centella Asiatica Extract, Hydrolyzed Hyaluronic Acid, Hydrolyzed Sodium Hyaluronate, Dimethylsilanol Hyaluronatem Sodium Hyaluronate, Hyaluronic Acid, Potassium Hyaluronate, Cyanocobalamin, Sodium Hyaluronate Crosspolymer, Hydroxypropyltrimonium Hyaluronate, Acetyl Hexapeptide-8, Sodium Hyaluronate Dimethylsilanol, Sodium Acetylated Hyaluronate, Menadione, Linolenic Acid

OTHER SAFETY INFORMATION

Protect the product in the container from excessive heat and direct sun.

Sun alaert: Limiting sun exposure, wearing protective clothing, and using suncreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SUNGBOON EDITOR DAILY INVISIBLE BLURRING SUNSCREEN 
avobenzone, homosalate, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85037-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	49 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	90 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	29 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ISODODECANE (UNII: A8289P68Y2)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
DIMETHICONE/BIS-ISOBUTYL PPG-20 CROSSPOLYMER (UNII: O4I3UFO6ZF)
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
POLYGLYCERYL-4 OLEATE (UNII: 15B05TY4GX)
WATER (UNII: 059QF0KO0R)
C12-13 PARETH-9 (UNII: 9BXD858P37)
POLYGLYCERYL-6 OLEATE (UNII: G4AYJ54K59)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
TOCOPHEROL (UNII: R0ZB2556P8)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SUNFLOWER OIL (UNII: 3W1JG795YI)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLUTATHIONE (UNII: GAN16C9B8O)
NIACINAMIDE (UNII: 25X51I8RD4)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PANTHENOL (UNII: WV9CM0O67Z)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
HIPPOPHAE RHAMNOIDES FRUIT (UNII: AVL0R9111T)
ORANGE (UNII: 5EVU04N5QU)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
DIMETHYLSILANOL HYALURONATE (UNII: Z853O1D4TE)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
HYALURONIC ACID (UNII: S270N0TRQY)
CYANOCOBALAMIN (UNII: P6YC3EG204)
ACETYL HEXAPEPTIDE-8 AMIDE (UNII: L4EL31FWIL)
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
MENADIONE (UNII: 723JX6CXY5)
LINOLENIC ACID (UNII: 0RBV727H71)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85037-002-02	1 in 1 CARTON	03/25/2025
1	NDC: 85037-002-01	50 mL in 1 TUBE; 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	03/25/2025

Labeler - Olive International Inc. (695818354)

Registrant - Olive International Inc. (695818354)

Establishment
Name	Address	ID/FEI	Business Operations
Rebom Co., Ltd.		695951708	manufacture(85037-002)