FDA.reportPublic FDA data

TRUFFLE EX TREATMENT

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2012-09-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:45:38

Label at a glance#

ProductTRUFFLE EX TREATMENT
Active ingredientWITCH HAZEL
Label structure8 sections

Indications and uses

How to Use: After washing your face, before or after applying our toner, dispense one drop onto your palm and gently rub your hands together. Softly massage with your palms to enhance its absorption into your skin.

Dosage and administration

How to Use: After washing your face, before or after applying our toner, dispense one drop onto your palm and gently rub your hands together. Softly massage with your palms to enhance its absorption into your skin.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: WITCH HAZEL 0.05%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
CETEARYL ETHYLHEXANOATE, CYCLOPENTASILOXANE, CAPRYLIC/CAPRIC TRIGLYCERIDE, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, GLYCERYL CAPRYLATE, CAPRYLYL GLYCOL, LIMNANTHES ALBA (MEADOWFOAM) SEED OIL, MACADAMIA TERNIFOLIA SEED OIL, TUBER MELANOSPORUM EXTRACT, AGARICUS BISPORUS (MUSHROOM) EXTRACT, CORTHELLUS SHIITAKE (MUSHROOM) EXTRACT, GANODERMA LUCIDUM (MUSHROOM) EXTRACT, HERICIUM ERINACEUM (MUSHROOM) EXTRACT, INONOTUS OBLIQUUS (MUSHROOM) EXTRACT, PHELLINUS LINTEUS EXTRACT, PLEUROTUS OSTREATUS (MUSHROOM) EXTRACT, SARCODON ASPRATUS EXTRACT, TRAMETES VERSICOLOR EXTRACT, TREMELLA FUCIFORMIS (MUSHROOM) EXTRACT, ARTEMISIA ABSINTHIUM EXTRACT, VANILLA PLANIFOLIA FRUIT EXTRACT, SALMON EGG EXTRACT, CITRUS AURANTIUM BERGAMIA (BERGAMOT) FRUIT OIL, OLEA EUROPAEA (OLIVE) FRUIT OIL, CITRUS AURANTIUM DULCIS (ORANGE) OIL, CITRUS GRANDIS (GRAPEFRUIT) PEEL OIL, WATER, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, CEDRUS ATLANTICA BARK OIL,
PELARGONIUM GRAVEOLENS FLOWER OIL, BUTYLENE GLYCOL, COPAIFERA OFFICINALIS (BALSAM COPAIBA) RESIN, JASMINUM OFFICINALE (JASMINE) OIL, MYRTUS COMMUNIS OIL, ROSE FLOWER OIL, FERULA GALBANIFLUA (GALBANUM) RESIN OIL, 1,2-HEXANEDIOL, ETHYLHEXYLGLYCERIN, TROPOLONE

PURPOSE

OTC - PURPOSE SECTION

Purpose: A treatment oil that is abundant with the nutrients from truffle mushroom extracts.

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 your face, before or after applying our toner, dispense one drop onto your palm and gently rub your hands together. Softly massage with your palms to enhance its absorption into your skin.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use:
After washing your face, before or after applying our toner, dispense one drop onto your palm and gently rub your hands together. Softly massage with your palms to enhance its absorption into your skin.

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
51346-157-012021-07-09C16284748780-19d75b9d1-0ab3-f424-e053-dadaa90a57cec5d1fd9c-187a-4741-bb37-33978f6e8e4a
51346-157-012020-01-31C16284748780-19d75b9d1-0ab3-f424-e053-dadaa90a57cec5d1fd9c-187a-4741-bb37-33978f6e8e4a

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
WITCH HAZELACTIVE INGREDIENT101I4J0U341
WITCH HAZELACTIVE MOIETY101I4J0U341
CAPRYLYL GLYCOLINACTIVE INGREDIENT00YIU5438U1
CETEARYL ETHYLHEXANOATEINACTIVE INGREDIENT9M64UO4C251
GLYCERYL CAPRYLATEINACTIVE INGREDIENTTM2TZD4G4A1
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
51346-15751346-157-01

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
WITCH HAZEL101I4J0U34ACTIM
CETEARYL ETHYLHEXANOATE9M64UO4C25IACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
CAPRYLYL GLYCOL00YIU5438UIACT
WATER059QF0KO0RIACT

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
GLYCERYL CAPRYLATEGLYCERYL MONOCAPRYLATETM2TZD4G4ATABLET / ORAL1 mgExact identifier — unii candidate
2 equally ranked IID candidates
GLYCERYL CAPRYLATEGLYCERYL MONOCAPRYLATETM2TZD4G4ACAPSULE / ORAL400 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
65f0b314-5b87-4dc7-bac5-18afa54474e8c5d1fd9c-187a-4741-bb37-33978f6e8e4a2021-07-08WarningsExact identifier
spl set id: c5d1fd9c-187a-4741-bb37-33978f6e8e4a

Reported adverse events (FAERS/openFDA)#

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