FDA.reportPublic FDA data

SOLIE ESSENCE

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 01:45:51

Label at a glance#

ProductSOLIE ESSENCE
Active ingredientGLYCERIN
Label structure8 sections

Indications and uses

How to Use: After using toner, pump out a small amount and apply gently over face.

Dosage and administration

How to Use: After using toner, pump out a small amount and apply gently over face.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: GLYCERIN 20%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
WATER, BUTYLENE GLYCOL, HONEY EXTRACT, PANAX GINSENG ROOT EXTRACT, CETEARYL ALCOHOL, HYDROGENATED POLYISOBUTENE, CARTHAMUS TINCTORIUS (SAFFLOWER) FLOWER EXTRACT, CHRYSANTHELLUM INDICUM EXTRACT, OENOTHERA BIENNIS (EVENING PRIMROSE) FLOWER EXTRACT, PRUNUS MUME FLOWER EXTRACT, PRUNUS SERRULATA FLOWER EXTRACT, HYDROGENATED LECITHIN, 1,2-HEXANEDIOL, ALCOHOL, ARCTIUM LAPPA ROOT EXTRACT, PHELLINUS LINTEUS EXTRACT, SODIUM STEAROYL GLUTAMATE, C12-13 PARETH-23, DIVINYLDIMETHICONE/DIMETHICONE COPOLYMER, PHENOXYETHANOL, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, FRAGRANCE,
CARBOMER, C12-13 PARETH-3, CHAENOMELES SINENSIS FRUIT EXTRACT, CITRUS JUNOS FRUIT EXTRACT, CORNUS OFFICINALIS FRUIT EXTRACT, PONCIRUS TRIFOLIATA FRUIT EXTRACT, PRUNUS MUME FRUIT EXTRACT, PUNICA GRANATUM FRUIT EXTRACT, SCHIZANDRA CHINENSIS FRUIT EXTRACT, POTASSIUM HYDROXIDE, ETHYLHEXYLGLYCERIN, PANTHENOL, SODIUM HYALURONATE, ADENOSINE, CARAMEL, DISODIUM EDTA, PROPYLENE GLYCOL, RAFFINOSE, OPUNTIA COCCINELLIFERA, SOLUBLE COLLAGEN, XANTHAN GUM, FOLIC ACID, CERAMIDE 3, CHOLESTEROL, ACACIA SENEGAL GUM, TROMETHAMINE, PALMITOYL PENTAPEPTIDE-4

PURPOSE

OTC - PURPOSE SECTION

Purpose: A highly concentrated Korean traditional herbal essence 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 using toner, pump out a small amount and apply gently over face.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use: After using toner, pump out a small amount and apply gently 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
51346-089-012021-06-30C16284748780-19d75b9d0-1d68-f424-e053-dadaa90a57ce0af77860-648c-4a49-ba32-3cf07e863edb
51346-089-012020-01-31C16284748780-19d75b9d0-1d68-f424-e053-dadaa90a57ce0af77860-648c-4a49-ba32-3cf07e863edb

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GLYCERINACTIVE INGREDIENTPDC6A3C0OX1
GLYCERINACTIVE MOIETYPDC6A3C0OX1
1,2-HEXANEDIOLINACTIVE INGREDIENTTR046Y3K1G1
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 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-08951346-089-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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

Source Document#

Source XML · Source PDF

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
790f3fad-9edd-476d-bfdd-c65ac53510310af77860-648c-4a49-ba32-3cf07e863edb2021-06-29WarningsExact identifier
spl set id: 0af77860-648c-4a49-ba32-3cf07e863edb

Reported adverse events (FAERS/openFDA)#

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