FDA.reportPublic FDA data

TONYMOLY My Sunny All SunSpray

Manufacturer
Tonymoly Co., Ltd. | Cosmax, Inc.
Effective date
2016-02-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:44:51

Label at a glance#

ProductTONYMOLY My Sunny All SunSpray
Active ingredientTITANIUM DIOXIDE, OCTOCRYLENE
Label structure8 sections

Dosage and administration

After fully shaking the bottle, spray for 2-3 seconds from a distance of 20 cm on skin areas exposed to UV rays.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethylhexyl Methoxycinnamate 7.30%, Octocrylene 3.00%, Titanium Dioxide 3.24%, Zinc Oxide 4.32%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Use

DOSAGE & ADMINISTRATION SECTION

Sunscreen

Caution

WARNINGS SECTION

For external use only. Avoid contact with eyes. Keep out of reach of children. Discontinue use if signs of irritation and/or rash appear.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

INDICATIONS & USAGE SECTION

After fully shaking the bottle, spray for 2-3 seconds from a distance of 20 cm on skin areas exposed to UV rays.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cyclopentasiloxane, Cyclohexasiloxane, Alcohol Denat., Butylene Glycol, Methyl Methacrylate Crosspolymer, Ethylhexyl Palmitate, PEG-10 Dimethicone, Silica, Neopentyl Glycol Diheptanoate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Caprylyl Methicone, Aluminum Hydroxide, Glyceryl Caprylate, Stearic Acid, Disteardimonium Hectorite, Fragrance(Parfum), Dimethicone/Methicone Copolymer, Caprylyl Glycol, Disodium EDTA, Water, Phenoxyethanol, Prunus Mume Fruit Water, Nymphaea Alba Flower Extract, Aloe Barbadensis Leaf Extract, 1,2-Hexanediol, Origanum Vulgare Leaf Extract, Salix Alba (Willow) Bark Extract, Chamaecyparis Obtusa Leaf Extract, Ethylhexylglycerin, Portulaca Oleracea Extract, Cinnamomum Cassia Bark Extract, Scutellaria Baicalensis Root Extract, Lactobacillus/Soybean Ferment Extract, Polymethylsilsesquioxane, Platinum Powder

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sun spraysun spray

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59078-120-012023-01-30C16284748780-1f386c649-ff60-0266-e053-dadaa90a7c1a29cc6b6a-f476-1234-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59078-120-01TONYMOLY My Sunny All SunSpray150 mL in 1 BOTTLE, SPRAYSPRAY1503
59078-120-01TONYMOLY My Sunny All SunSpray1 in 1 CARTONSPRAY13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59078-120TONYMOLY MY SUNNY ALL SUNSPRAY (ETHYLHEXYL METHOXYCINNAMATE) SPRAY [TONYMOLY CO., LTD.]3Legacy NDC, 2 package rows20160204_29cc6b6a-f476-1234-e054-00144ff88e88.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59078-12059078-120-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Name, UNII, Kind table
NameUNIIKind
BEMOTRIZINOLPWZ1720CBHIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
EDETATE DISODIUM7FLD91C86KIACT
ALOE VERA LEAFZY81Z83H0XIACT
PORTULACA OLERACEA WHOLED5J3623SV2IACT
CHINESE CINNAMONWS4CQ062KMIACT
NYMPHAEA ALBA FLOWER40KQ7Q535OIACT
OREGANO0E5AT8T16UIACT
WILLOW BARKS883J9JDYXIACT
PLATINUM49DFR088MYIACT
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
GLYCERYL CAPRYLATETM2TZD4G4AIACT
OCTOCRYLENE5A68WGF6WMACTIB
BUTYLENE GLYCOL3XUS85K0RAIACT
ETHYLHEXYL PALMITATE2865993309IACT
STEARIC ACID4ELV7Z65APIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
CAPRYLYL GLYCOL00YIU5438UIACT
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CYCLOMETHICONE 50THT5PCI0RIACT
ALCOHOL3K9958V90MIACT
PRUNUS MUME FRUIT639190I8CUIACT
CHAMAECYPARIS OBTUSA LEAF7OL154J5XBIACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2af68f0b-4b4d-5387-e054-00144ff8d46c29cc6b6a-f476-1234-e054-00144ff88e882016-02-04WarningsExact identifier
spl id: 2af68f0b-4b4d-5387-e054-00144ff8d46c
spl set id: 29cc6b6a-f476-1234-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.