DHT X

Manufacturer
IDOOGEN Co.,Ltd.
Effective date
2019-12-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:50:11

Label at a glance#

ProductDHT X HAIRLOSS
Active ingredientNiacinamide
Label structure8 sections

Dosage and administration

DOSAGE AND ADMINISTRATION: Take an adequate amount of this product

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT: Niacinamide 0.3%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS:
Zinc Pyrithione, Panthenol, Niacinamide, Biotin, Acorus Calamus Root Extract, Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Citric Acid, Cocamide DEA, Cocamidopropyl Betaine, Copper Tripeptide-1, Dimethicone, Disodium EDTA, Fragrance, Guar Hydroxypropyltrimonium Chloride, Menthol, Methylchloroisothiazolinone and Methylisothiazolinone Mixed Solution, Polygonum Multiflorum Root Extract, Polyquaternium-10, Water

PURPOSE

OTC - PURPOSE SECTION

PURPOSE: Skin Protectant

WARNINGS

WARNINGS SECTION

WARNINGS:
1. It is not used in the following cases. Skin and scalp there is a skin wound or mucous membrane, such as eczema, damaged
2. Be discontinued immediately the use of this product in the following cases, consult your doctor or pharmacist, at the time of consultation, as far as possible : If rash, erythema, itching, swelling, and the like are displayed
3. Avoid contact with eyes.  If product gets into the eyes rinse well with water immediately.  it is recommended that you consult with an ophthalmologist if symptoms are severe
- For external use only
4. Keep out of reach of babies and children
- Do not store near high heat or flame
- Do not keep it in the place where the temperature is extremely hot or low and exposed the direct sunlight.
- Do not put in other containers for prevent abuse and keep quality

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of babies and children

INDICATION AND USAGE

INDICATIONS & USAGE SECTION

INDICATION AND USAGE:
Apply 3 to 5ml to wet hair and lather onto hair and scalp for 3mins. Rinse thoroughly with water to remove

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

DOSAGE AND ADMINISTRATION:
Take an adequate amount of this product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of cartonImage of cartonImage of carton

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
NiacinamideACTIVE INGREDIENT25X51I8RD41
NIACINAMIDEACTIVE MOIETY25X51I8RD41
PANTHENOLINACTIVE INGREDIENTWV9CM0O67Z1
PYRITHIONE ZINCINACTIVE INGREDIENTR953O2RHZ51

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
69281-03069281-030-01

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
Niacinamide25X51I8RD4ACTIB
PYRITHIONE ZINCR953O2RHZ5IACT
PANTHENOLWV9CM0O67ZIACT

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
9f203541-8cc0-48b9-8a3b-60e160be71e912e96e1d-52b2-4ea9-a419-9496e95474562021-05-28WarningsExact identifier
spl set id: 12e96e1d-52b2-4ea9-a419-9496e9547456

Reported adverse events (FAERS/openFDA)#

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