FDA.reportPublic FDA data

Biotin

Manufacturer
Shenzhen yuehaotong Technology Co.,Ltd
Effective date
2026-03-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:49:16

Label at a glance#

ProductBiotin
Active ingredientMINOXIDIL
Label structure11 sections

Label contents#

Full prescribing information#

COMPONENTS

Salicylic acid 2%

OTC - PURPOSE SECTION

wart remover

INDICATIONS & USAGE SECTION

Apply twice daly(moring and night as a man and once as a woman.Afer apicaion, proeed with an acive masage for 3-5 minutes unthe product is fuy absorbed

WARNINGS SECTION

Forevemaluseony Avoid coniac wth eves li coniac ocus nse ihorouthly wt waier Keep out ofreach oi chidrenifvou ale preanant.nursing. otiaveanyunderving medca condion.consutyou healthcare provider before using the product

DOSAGE & ADMINISTRATION SECTION

For external use only.

OTC - DO NOT USE SECTION

Discontinue use if any irritation or adverse reaction occurs

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes. lf contact occurs, rinse thoroughly with waterDiscontinue use if any irritation or adverse reaction occurs.

OTC - STOP USE SECTION

on broken or irritated scalp

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If sxralowed, get medical help or contact a Poison Conirol Cenler ngiht away.

INACTIVE INGREDIENT SECTION

Acrylates copolymer, Ethyl acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
MINOXIDIL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87492-002-01Biotin5 mL in 1 BOXLIQUID51
87492-002-02Biotin15 mL in 1 BOXLIQUID151
87492-002-03Biotin30 mL in 1 BOXLIQUID301
87492-002-04Biotin50 mL in 1 BOXLIQUID501
87492-002-05Biotin100 mL in 1 BOXLIQUID1001

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87492-00287492-002-01, 87492-002-02, 87492-002-03, 87492-002-04, 87492-002-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
SESAME OILQX10HYY4QVIACT
CHLORPHENESINI670DAL4SZIACT
PALMITOYL TETRAPEPTIDE-7Q41S464P1RIACT
MINOXIDIL5965120SH1ACTIB
PANTOTHENIC ACID19F5HK2737IACT
PALMITOYL TRIPEPTIDE-1RV743D216MIACT

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
BiotinBIOTINShenzhen yuehaotong Technology Co.,Ltd4c6ec616-a84e-6e1a-e063-6294a90a2aae2026-03-07WarningsExact identifier
ndc (package): 87492-002-05
ndc (package): 87492-002-03
ndc (package): 87492-002-01
ndc (package): 87492-002-02
ndc (package): 87492-002-04
ndc (product): 87492-002
ndc11 (package): 87492000205
ndc11 (package): 87492000201
ndc11 (package): 87492000202
ndc11 (package): 87492000204
ndc11 (package): 87492000203
spl id: 4c6ec616-a84f-6e1a-e063-6294a90a2aae
spl set id: 4c6ec616-a84e-6e1a-e063-6294a90a2aae

Reported adverse events (FAERS/openFDA)#

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