DEWYTREE URBAN SHADE HYALURONIC LIGHTWEIGHT SUNSCREEN- octocrylene, homosalate, octisalate, avobenzone cream

DEWYTREE URBAN SHADE HYALURONIC LIGHTWEIGHT SUNSCREEN by

Drug Labeling and Warnings

DEWYTREE URBAN SHADE HYALURONIC LIGHTWEIGHT SUNSCREEN by is a Otc medication manufactured, distributed, or labeled by DEWYTREE CO. ,LTD, reBom Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Octocrylene 9.8%

Homosalate 7.2%

Octisalate 4.8%

Avobenzone 3.0%

PURPOSE

Sunscreen

INDICATIONS & USAGE

■ Helps prevent sunburn. ■ if used as directed with other sun protection measures ( see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

WARNINGS

■ For external use only.

DO NOT USE

Do not use ■ on damaged or broken skin.

STOP USE

Stop use and ask a doctor if ■ rash occurs.

WHEN USING

When using this product ■ keep out of eyes. Rinse with water to remove.

KEEP OUT OF REACH OF CHILDREN

■ Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

DOSAGE & ADMINISTRATION

Directions

■ Apply liberally 15 minutes before sun exposure. ■ Reapply at least every 2 hours. ■ Children under 6 months of age: Ask a doctor. ■ 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 value of 15 or higher and other sun protection measures including: ■ limit time in the sun, especially from 10a.m.-2 p.m. wear long-sleeve shirts, pants, hats, and sunglasses.

OTHER SAFETY INFORMATION

■ protect this product in this container from excessive heat and direct sun.

INACTIVE INGREDIENT

Water(Aqua), Isohexadecane, Dipropylene Glycol, Silica, Niacinamide, Cetearyl Glucoside, Sorbitan Olivate, Benzyl Glycol, Panthenol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Arginine, Cetearyl Alcohol, Xanthan Gum, Pentylene Glycol, Adenosine, Ethylhexylgly cerin, Mentha Piperita (Peppermint) Oil, Squalane, Ganoderma Lucidum (Mushroom) Stem Extract, Butylene Glycol, 1,2-Hexanediol, Hydrolyzed Hyaluronic Acid, Hydrolyzed Sodium Hyaluronate, Dimethylsilanol Hyaluronate, Sodium Hyaluronate, Hyaluronic Acid, Potassium Hyaluronate, Sodium Hyaluronate Crosspolymer, Hydroxypropyltrimonium Hyaluronate, Sodium Hyaluronate Dimethylsilanol, Sodium Acetylated Hyaluronate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DEWYTREE URBAN SHADE HYALURONIC LIGHTWEIGHT SUNSCREEN 
octocrylene, homosalate, octisalate, avobenzone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73071-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	2.4 g  in 50 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	3.6 g  in 50 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	4.9 g  in 50 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	1.5 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
ARGININE (UNII: 94ZLA3W45F)
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
SQUALANE (UNII: GW89575KF9)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
NIACINAMIDE (UNII: 25X51I8RD4)
ADENOSINE (UNII: K72T3FS567)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
DIMETHYLSILANOL HYALURONATE (UNII: Z853O1D4TE)
PANTHENOL (UNII: WV9CM0O67Z)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
SILICA (UNII: ETJ7Z6XBU4)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
SORBITAN OLIVATE (UNII: MDL271E3GR)
BENZYL GLYCOL (UNII: 06S8147L47)
GANODERMA LUCIDUM STEM (UNII: U8PA41532G)
XANTHAN GUM (UNII: TTV12P4NEE)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
WATER (UNII: 059QF0KO0R)
ISOHEXADECANE (UNII: 918X1OUF1E)
MENTHA PIPERITA (PEPPERMINT) OIL (UNII: AV092KU4JH)
HYALURONIC ACID (UNII: S270N0TRQY)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73071-101-01	1 in 1 BOX	03/26/2025
1	NDC: 73071-101-02	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	03/26/2025

Labeler - DEWYTREE CO. ,LTD (688358542)

Establishment
Name	Address	ID/FEI	Business Operations
reBom Co., Ltd.		695951708	manufacture(73071-101)