HYUNDAE MEDITECH BIO HAIR SOLU TION ERUA DO

Manufacturer
INNOGENE CO.,LTD
Effective date
2016-10-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:47:21

Label at a glance#

ProductHYUNDAE MEDITECH BIO HAIR SOLU TION ERUA DO
Active ingredientAllantoin
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Allantoin 0.95%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Glycerin, Butylene Glycol, Methylparaben, Phenoxyethanol, Sorbitol, Glycogen, Copper Tripeptide-1, Mannitol, Pterocarpus Marsupium Bark Extract, Serenoa Serrulata Fruit Extract, Ammonium Glycyrrhizate, Disodium Succinate, Eriobotrya Japonica Leaf Extract, Glutamic Acid, Caffeine, Zinc Gluconate, Aesculus Hippocastanum (Horse Chestnut) Seed Extract

PURPOSE

OTC - PURPOSE SECTION

Purpose: Scalp Protectant

WARNINGS

WARNINGS SECTION

Warnings: 1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms): a) Red spots, swelling, itchiness, and other skin irritation b) If the symptoms above occur after the application area is exposed to direct sunlight. 2. Do not use on open wounds, eczema, and other skin irritations. 3. Storing and handling a) Close the lid after every use. b) Keep out of reach of infants and children. c) Do not store at extreme temperatures or in an area exposed to direct sunlight. 4. Wash away immediately when permeating into the eyes.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of infants and children.

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & usage: 1. Wash scalp tholoughly before product use. 2. Shake the product. 3. Take appropriate amount out of a container and rub on parts of scalp in trouble to absorb enough.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: One time per week, 5cc for one use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70540-030-022020-01-31C16284748780-19d75b9d1-11bb-f424-e053-dadaa90a57ce01c82eea-de63-4e92-a62e-88fcf0108875

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70540-030-01HYUNDAE MEDITECH BIO HAIR SOLU TION ERUA DO5 g in 1 VIALSOLUTION51
70540-030-02HYUNDAE MEDITECH BIO HAIR SOLU TION ERUA DO12 in 1 CARTONSOLUTION121

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70540-030HYUNDAE MEDITECH BIO HAIR SOLU TION ERUA DO (ALLANTOIN) SOLUTION [INNOGENE CO.,LTD]1Legacy NDC, 2 package rows20161005_01c82eea-de63-4e92-a62e-88fcf0108875.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70540-03070540-030-01, 70540-030-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
Allantoin344S277G0ZACTIB
Water059QF0KO0RIACT
GlycerinPDC6A3C0OXIACT

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
245220e7-cc83-4f8f-a01b-acf72e6c59c101c82eea-de63-4e92-a62e-88fcf01088752016-10-05WarningsExact identifier
spl id: 245220e7-cc83-4f8f-a01b-acf72e6c59c1
spl set id: 01c82eea-de63-4e92-a62e-88fcf0108875

Reported adverse events (FAERS/openFDA)#

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