FDA.reportPublic FDA data

SOLIE TONER

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2012-09-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:45:55

Label at a glance#

ProductSOLIE TONER
Active ingredientGLYCERIN, ALLANTOIN
Label structure8 sections

Indications and uses

How to Use: After washing, use a cotton pad to gently wipe toner over face.

Dosage and administration

How to Use: After washing, use a cotton pad to gently wipe toner over face.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: GLYCERIN 20%, ALLANTOIN 0.5%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
WATER, HONEY EXTRACT, PANAX GINSENG ROOT EXTRACT, BUTYLENE GLYCOL, BETAINE, CARTHAMUS TINCTORIUS (SAFFLOWER) FLOWER EXTRACT, CHRYSANTHELLUM INDICUM EXTRACT, OENOTHERA BIENNIS (EVENING PRIMROSE) FLOWER EXTRACT, PRUNUS MUME FLOWER EXTRACT, PRUNUS SERRULATA FLOWER EXTRACT, PEG-60 HYDROGENATED CASTOR OIL, 1,2-HEXANEDIOL, ARCTIUM LAPPA ROOT EXTRACT, PHELLINUS LINTEUS EXTRACT, CAPRYLIC/CAPRIC TRIGLYCERIDE, PHENOXYETHANOL, TROMETHAMINE, CARBOMER, CENTELLA ASIATICA EXTRACT, FICUS CARICA (FIG) FRUIT EXTRACT, POLYSORBATE 60, CHAENOMELES SINENSIS FRUIT EXTRACT, CITRUS JUNOS FRUIT EXTRACT,
CORNUS OFFICINALIS FRUIT EXTRACT, OPUNTIA COCCINELLIFERA, PONCIRUS TRIFOLIATA FRUIT EXTRACT, PRUNUS MUME FRUIT EXTRACT, PUNICA GRANATUM FRUIT EXTRACT, SCHIZANDRA CHINENSIS FRUIT EXTRACT, FRAGRANCE, ETHYLHEXYLGLYCERIN, DIPOTASSIUM GLYCYRRHIZATE, HYDROGENATED LECITHIN, ADENOSINE, DISODIUM EDTA, SODIUM POLYACRYLATE, STEARETH-21, SODIUM HYALURONATE, CARAMEL, CETYL ALCOHOL, STEARETH-2, ISOHEXADECANE, STEARIC ACID, RAFFINOSE, SOLUBLE COLLAGEN, XANTHAN GUM, PROPYLENE GLYCOL, CELLULOSE GUM, PEG-30 DIPOLYHYDROXYSTEARATE, ACACIA SENEGAL GUM, TOCOPHERYL ACETATE, CERAMIDE 3, GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER, PALMITOYL PENTAPEPTIDE-4, YELLOW 6, METHYLISOTHIAZOLINONE

PURPOSE

OTC - PURPOSE SECTION

Purpose: A highly concentrated Korean traditional herbal fluid containing Korean ginseng and five kinds of honey rich in nutrition and moisture to maintain the natural moisture and nutrition of your skin and leave it clearer and more vibrant.

WARNINGS

WARNINGS SECTION

Cautions:
For external use only.
Avoid contact with eyes and mouth.
Discontinue use if signs of irritation or rash appear.
Keep out of reach of children.
Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

How to Use: After washing, use a cotton pad to gently wipe toner over face.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use: After washing, use a cotton pad to gently wipe toner over face.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-087-012021-06-30C16284748780-19d75b9d0-9850-f424-e053-dadaa90a57cefb5d4c27-cc2a-4e8e-8248-2930dc78214b
51346-087-012020-01-31C16284748780-19d75b9d0-9850-f424-e053-dadaa90a57cefb5d4c27-cc2a-4e8e-8248-2930dc78214b

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALLANTOINACTIVE INGREDIENT344S277G0Z1
GLYCERINACTIVE INGREDIENTPDC6A3C0OX1
ALLANTOINACTIVE MOIETY344S277G0Z1
GLYCERINACTIVE MOIETYPDC6A3C0OX1
1,2-HEXANEDIOLINACTIVE INGREDIENTTR046Y3K1G1
BETAINEINACTIVE INGREDIENT3SCV180C9W1
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RA1
HONEYINACTIVE INGREDIENTY9H1V576FH1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-08751346-087-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXACTIM
ALLANTOIN344S277G0ZACTIM
WATER059QF0KO0RIACT
HONEYY9H1V576FHIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
BETAINE3SCV180C9WIACT
1,2-HEXANEDIOLTR046Y3K1GIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
aaad36a5-0bba-4bdb-a214-93c69b7acf16fb5d4c27-cc2a-4e8e-8248-2930dc78214b2021-06-29WarningsExact identifier
spl set id: fb5d4c27-cc2a-4e8e-8248-2930dc78214b

Reported adverse events (FAERS/openFDA)#

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