SUNGBOON EDITOR HYDRO BOOSTER MOISTURE SUNSCREEN- homosalate, octisalate, octocrylene, avobenzone cream

Sungboon Editor Hydro Booster Moisture Sunscreen by

Drug Labeling and Warnings

Sungboon Editor Hydro Booster Moisture Sunscreen by is a Otc medication manufactured, distributed, or labeled by Olive International Co., Ltd., Rebom Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Avobenzone 2.8%

Homosalate 12%

Octisalate 4.8%

Octocrylene 4.5%

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

Water, Dipropylene Glycol, Cyclopentasiloxane, Niacinamide, Butyloctyl Salicylate, Cyclohexasiloxane, Benzyl Glycol, Pentylene Glycol, Polymethylsilsesquioxane, Silica, Glyceryl Stearate, PEG-100 Stearate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Arginine, Betaine, Panthenol, Glycerin, Ganoderma Lucidum (Mushroom) Stem Extract, Ethylhexylglycerin, Xanthan Gum, Hydroxypropyl Methylcellulose Stearoxy Ether, Adenosine, Butylene Glycol, Pyrus Communis (Pear) Fruit Extract, 1,2-Hexanediol, Rosa Damascena Flower Water, Allantoin, Caffeine, Acacia Senegal Flower/Stem Extract, Iris Florentina Root Extract, Cucumis Melo (melon) Fruit Extract, Hydrolyzed Collagen, Hydrogenated lecithin, Hedera Helix (Ivy) Leaf/Stem Extract, Cetearyl Alcohol, Stearic Acid, Centella Asiatica Extract, Ethyl Hexanediol, Hydrolyzed Elastin, Palmitoyl Tripeptide-5, Hydrolyzed Hyaluronic Acid, Hydrolyzed Sodium Hyaluronate, Dimethylsilanol Hyaluronate, Sodium Hyaluronate, Hyaluronic Acid, Hydrolyzed Collagen Extract, Potassium Hyaluronate, Sodium Hyaluronate Crosspolymer, Hydroxypropyltrimonium Hyaluronate, Ceramide NP, Sodium Hyaluronate Dimethylsilanol, Sodium Acetylated Hyaluronate, Cholesterol, Phytosphingosine, Ceramide NG, Ceramide NS, Ceramide AS, Ceramide AP, Collagen Extract, Ceramide EOP

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 HYDRO BOOSTER MOISTURE SUNSCREEN 
homosalate, octisalate, octocrylene, avobenzone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85037-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	120 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	48 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	45 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	28 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
NIACINAMIDE (UNII: 25X51I8RD4)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
ETHYLENE GLYCOL MONOBENZYL ETHER (UNII: 06S8147L47)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 MONOSTEARATE (UNII: YD01N1999R)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S AT 0.5%) (UNII: YY2HMJ9NZF)
ARGININE (UNII: 94ZLA3W45F)
BETAINE (UNII: 3SCV180C9W)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
PANTHENOL (UNII: WV9CM0O67Z)
GLYCERIN (UNII: PDC6A3C0OX)
GANODERMA LUCIDUM STEM (UNII: U8PA41532G)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
XANTHAN GUM (UNII: TTV12P4NEE)
HYPROMELLOSE 2208 0.45% STEAROXY ETHER (UNII: MG58AH4FJ8)
ADENOSINE (UNII: K72T3FS567)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PEAR (UNII: 2ZN8DWC0YF)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ROSA X DAMASCENA FLOWER OIL (UNII: 18920M3T13)
ALLANTOIN (UNII: 344S277G0Z)
CAFFEINE (UNII: 3G6A5W338E)
SENEGALIA SENEGAL FLOWER (UNII: 72P931MTC2)
IRIS X GERMANICA NOTHOVAR. FLORENTINA ROOT (UNII: M30XO5X4XD)
MUSKMELON (UNII: ZV095H5633)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
HEDERA HELIX TOP (UNII: ZP9XFG71A7)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
STEARIC ACID (UNII: 4ELV7Z65AP)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
ETHOHEXADIOL (UNII: M9JGK7U88V)
HYDROLYZED BOVINE ELASTIN (BASE; 1000 MW) (UNII: ZR28QKN0WT)
PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
DIMETHYLSILANOL HYALURONATE (UNII: Z853O1D4TE)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
HYALURONIC ACID (UNII: S270N0TRQY)
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)
CERAMIDE NP (UNII: 4370DF050B)
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
CHOLESTEROL (UNII: 97C5T2UQ7J)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
CERAMIDE NG (UNII: C04977SRJ5)
CERAMIDE NS (UNII: V7M2259XJM)
N-BUTYRYL-D-ERYTHRO-SPHINGOSINE (UNII: SF3LP91341)
CERAMIDE AP (UNII: F1X8L2B00J)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85037-001-02	1 in 1 CARTON	02/23/2025
1	NDC: 85037-001-01	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	02/23/2025

Labeler - Olive International Co., Ltd. (695818354)

Registrant - Olive International Co., Ltd. (695818354)

Establishment
Name	Address	ID/FEI	Business Operations
Rebom Co., Ltd.		695951708	manufacture(85037-001)