FDA.reportPublic FDA data

Meori Toktok

Manufacturer
Kolive Cell Co., Ltd.
Effective date
2025-02-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:54:31

Label at a glance#

ProductMeori Toktok
Active ingredientBIOTIN, MENTHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Biotin, propolis

OTC - PURPOSE SECTION

Dandruff prevention, hair loss prevention and treatment, hair growth

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

take appropriate amount when scalp care

WARNINGS SECTION

Keep out of reach of infants and children

DOSAGE & ADMINISTRATION SECTION

take appropriate amount when scalp care

INACTIVE INGREDIENT SECTION

Salicylic acid, Goji berry, Eoseongcho, aloe, chaga mushroom, antler, cordyceps, red ginseng, rosemary

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83125-0001-12025-02-06C16284748780-11030e365-561c-111a-e063-dadaa90a10e2Drug Facts
83125-0001-12024-01-30C16284748780-11030e365-561c-111a-e063-dadaa90a10e2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83125-0001-1Meori Toktok100 mL in 1 BOTTLELIQUID1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83125-0001MEORI TOKTOK (BIOTINM PROPOLIS) LIQUID [KOLIVE CELL CO., LTD.]2Legacy NDC, 1 package rows20250207_ee696f39-03ed-8929-e053-2995a90a779f.zip

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
83125-000183125-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
SULFUR70FD1KFU70IACT
WATER059QF0KO0RIACT
BIOTIN6SO6U10H04ACTIB
MENTHOLL7T10EIP3AACTIB

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
2d734ce9-7f04-f176-e063-6394a90a7cbfee696f39-03ed-8929-e053-2995a90a779f2025-02-06WarningsExact identifier
spl id: 2d734ce9-7f04-f176-e063-6394a90a7cbf
spl set id: ee696f39-03ed-8929-e053-2995a90a779f

Reported adverse events (FAERS/openFDA)#

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