FDA.reportPublic FDA data

TONYMOLY My Sunny Watery Sun Gel

Manufacturer
Tonymoly Co., Ltd. | Kolmar
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 Watery Sun Gel
Active ingredientGLYCERIN
Label structure8 sections

Dosage and administration

During the last step of basic skin care, dispense an appropriate amount and evenly apply to any skin that will be exposed to ultraviolet sunlight.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethylhexyl Methoxycinnamate 6%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

DOSAGE & ADMINISTRATION SECTION

This oil-free sun gel has a watery texture that applies softly and lightly to the skin, without leaving any sticky residue behind.

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

During the last step of basic skin care, dispense an appropriate amount and evenly apply to any skin that will be exposed to ultraviolet sunlight.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

WATER, CYCLOPENTASILOXANE, ETHYLHEXYL SALICYLATE, ISOAMYL P-METHOXYCINNAMATE, BUTYLENE GLYCOL, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, TRIETHANOLAMINE, GLYCERIN, DIPROPYLENE GLYCOL, PEG/PPG-30/10 DIMETHICONE, CARBOMER, CAPRYLYL GLYCOL, C12-13 PARETH-23, DIVINYLDIMETHICONE/DIMETHICONE COPOLYMER, BEHENYL ALCOHOL, CETETH-10, FRAGRANCE, PHENOXYETHANOL, POLYMETHYLSILSESQUIOXANE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ALLANTOIN, CAPRYLHYDROXAMIC ACID, C12-13 PARETH-3, CHAMAECYPARIS OBTUSA LEAF EXTRACT, ORIGANUM VULGARE LEAF EXTRACT, SALIX ALBA (WILLOW) BARK EXTRACT, CINNAMOMUM CASSIA BARK EXTRACT, LACTOBACILLUS/SOYBEAN FERMENT EXTRACT, PORTULACA OLERACEA EXTRACT, SCUTELLARIA BAICALENSIS ROOT EXTRACT, NYMPHAEA ALBA FLOWER EXTRACT, ALOE BARBADENSIS LEAF JUICE, GLYCERYL POLYMETHACRYLATE, PROPYLENE GLYCOL, PLATINUM POWDER, POLYSORBATE 80

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

productproduct

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCERIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59078-122-012020-09-27C16284748780-1ab0e2407-3217-f274-e053-dbdaa90a647129ddb0ac-a375-1a20-e054-00144ff8d46c
59078-122-012020-09-25C16284748780-1ab0e2407-3217-f274-e053-dbdaa90a647129ddb0ac-a375-1a20-e054-00144ff8d46c
59078-122-012020-07-22C16284748780-1ab0e2407-3217-f274-e053-dbdaa90a647129ddb0ac-a375-1a20-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59078-122-01TONYMOLY My Sunny Watery Sun Gel45 g in 1 CONTAINERGEL453
59078-122-01TONYMOLY My Sunny Watery Sun Gel1 in 1 CARTONGEL13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59078-122TONYMOLY MY SUNNY WATERY SUN GEL (ETHYLHEXYL METHOXYCINNAMATE) GEL [TONYMOLY CO., LTD.]3Legacy NDC, 2 package rows20160204_29ddb0ac-a375-1a20-e054-00144ff8d46c.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
59078-12259078-122-01

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
TROLAMINE9O3K93S3TKIACT
OREGANO0E5AT8T16UIACT
CHINESE CINNAMONWS4CQ062KMIACT
NYMPHAEA ALBA FLOWER40KQ7Q535OIACT
ALOE VERA LEAFZY81Z83H0XIACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT
DIPROPYLENE GLYCOLE107L85C40IACT
CAPRYLYL GLYCOL00YIU5438UIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXACTIB
POLYSORBATE 806OZP39ZG8HIACT
ALLANTOIN344S277G0ZIACT
C12-13 PARETH-23J1WW1510L4IACT
C12-13 PARETH-3DMC6N3419LIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CETETH-10LF9X1PN3XJIACT
PEG/PPG-30/10 DIMETHICONEJ5JO20R8LHIACT
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATEANQ870JD20IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CYCLOMETHICONE 50THT5PCI0RIACT
AMILOXATE376KTP06K8IACT
CHAMAECYPARIS OBTUSA LEAF7OL154J5XBIACT
OCTISALATE4X49Y0596WIACT
DOCOSANOL9G1OE216XYIACT
WILLOW BARKS883J9JDYXIACT
PORTULACA OLERACEA WHOLED5J3623SV2IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PLATINUM49DFR088MYIACT

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
2af6e1bc-9945-188c-e054-00144ff88e8829ddb0ac-a375-1a20-e054-00144ff8d46c2016-02-04WarningsExact identifier
spl id: 2af6e1bc-9945-188c-e054-00144ff88e88
spl set id: 29ddb0ac-a375-1a20-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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