FDA.reportPublic FDA data

SUNTIQUE IM TONE UP MULTI BASE

Manufacturer
Normalest Co., Ltd. | COSON Co., Ltd._Osan Plant
Effective date
2020-07-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:22:54

Label at a glance#

ProductSUNTIQUE IM TONE UP MULTI BASE
Active ingredientOCTINOXATE, HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SUNTIQUE I'M TONE UP MULTI BASESUNTIQUE I'M TONE UP MULTI BASE

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Octyl Methoxycinnamate 7%

Homosalate 6%

Octyl Salicylate 4.5%

Titanium Dioxide 3.5%

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Dicaprylyl Carbonate, Propanediol, C12-15 Alkyl Benzoate, Cyclopentasiloxane, Glyceryl Stearate, PEG-100 Stearate, Polysorbate 60, Salvia Hispanica Seed Extract, Centella Asiatica Extract, Ammonium Acryloyldimethyltaurate/VP Copolymer, Houttuynia Cordata Extract, Pentylene Glycol, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Synthetic Fluorphlogopite, Methyl Methacrylate Crosspolymer, Phenoxyethanol, Squalane, Aluminum Stearate, Fragrance, Fructooligosaccharides, Polyhydroxystearic Acid, Saccharide, Hydrolysate, Pullulan, Alumina, 1,2-Hexanediol, Aluminum Hydroxide, Ethylhexylglycerin, Xanthan Gum, Octyldodecanol, Iron Oxides (CI 77492), Triethoxycaprylylsilane, Disodium EDTA, Sorbitan Isostearate, Iron Oxides (CI 77491), Echium Plantagineum Seed Oil, Butylene Glycol, Glycerin, Tin Oxide, Alcohol, Cardiospermum Halicacabum Flower/Leaf/Vine Extract, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, Achillea Millefolium Extract, Alchemilla Vulgaris Extract, Malva Sylvestris (Mallow) Extract ,Melissa Officinalis Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Primula Veris Extract, Veronica Officinalis Extract, Tocopherol, Sodium Hydroxide

OTC - ASK DOCTOR SECTION

OTC - ASK DOCTOR/PHARMACIST SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - PURPOSE SECTION

OTC - STOP USE SECTION

OTC - WHEN USING SECTION

WARNINGS SECTION

DOSAGE & ADMINISTRATION SECTION

OTHER SAFETY INFORMATION

STATEMENT OF IDENTITY SECTION

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72284-0012-12022-01-28C16284748780-1d6a99b39-7810-a426-e053-dadaa90af4c2SUNTIQUE I'M TONE UP MULTI BASE 120 mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72284-0012-1SUNTIQUE IM TONE UP MULTI BASE120 mL in 1 TUBELOTION1201
72284-0012-1SUNTIQUE IM TONE UP MULTI BASE1 in 1 BOXLOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72284-0012SUNTIQUE IM TONE UP MULTI BASE (HOMOSALATE, ETHYLHEXYL METHOXYCINNAMATE, ETHYLHEXYL SALICYLATE, TITANIUM DIOXIDE) LOTION [NORMALEST CO., LTD.]1Legacy NDC, 2 package rows20200728_ab7bade7-fed5-4f98-e053-2a95a90a9da2.zip

Products#

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

DailyMed product names page 1 of 2 · 54 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72284-001272284-0012-1

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 51 matching rows.

Name, UNII, Kind table
NameUNIIKind
SQUALANEGW89575KF9IACT
FOSFRUCTOSEM7522JYX1HIACT
INVERT SUGARED959S6ACYIACT
PULLULAN8ZQ0AYU1TTIACT
ALUMINUM OXIDELMI26O6933IACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
OCTYLDODECANOL461N1O614YIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
FERRIC OXIDE RED1K09F3G675IACT
GLYCERINPDC6A3C0OXIACT
STANNIC OXIDEKM7N50LOS6IACT
ACHILLEA MILLEFOLIUM2FXJ6SW4PKIACT
MELISSA OFFICINALIS LEAF50D2ZE9219IACT
MENTHA PIPERITA LEAFA389O33LX6IACT
TOCOPHEROLR0ZB2556P8IACT
SODIUM HYDROXIDE55X04QC32IIACT
OCTINOXATE4Y5P7MUD51ACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
WATER059QF0KO0RIACT
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATEANQ870JD20IACT
PROPANEDIOL5965N8W85TIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
CYCLOMETHICONE 50THT5PCI0RIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
POLYSORBATE 60CAL22UVI4MIACT
SALVIA HISPANICA SEEDNU0OLX06F8IACT
CENTELLA ASIATICA7M867G6T1UIACT
HOUTTUYNIA CORDATA WHOLEO3E12ZLW5TIACT
PENTYLENE GLYCOL50C1307PZGIACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%)86FQE96TZ4IACT
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER657L0NC5MTIACT
PHENOXYETHANOLHIE492ZZ3TIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
1,2-HEXANEDIOLTR046Y3K1GIACT

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
ab7baaca-46a0-c872-e053-2a95a90a5509ab7bade7-fed5-4f98-e053-2a95a90a9da22020-07-28Exact identifier
spl id: ab7baaca-46a0-c872-e053-2a95a90a5509
spl set id: ab7bade7-fed5-4f98-e053-2a95a90a9da2

Reported adverse events (FAERS/openFDA)#

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