83766-002 RHRTTUE 5% Minoxidil Applicator Pens

Manufacturer
Shenzhen Joyuflsh Technology Co.,Ltd.
Effective date
2026-04-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:53:46

Label at a glance#

ProductRHRTTUE 5% Minoxidil Applicator Pens
Active ingredientMINOXIDIL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%

OTC - PURPOSE SECTION

Targeted Hair Regrowth Treatment

INDICATIONS & USAGE SECTION

Use to regrow hair of the scalp and beard growth for men

WARNINGS SECTION

For external use only.
Keep out of reach of children.

OTC - DO NOT USE SECTION


You have no family history of hair loss.
Your hair loss is sudden and/or patchy.
Your hair loss is associated with childbirth.
You do not know the reason for your hair loss.
You are under 18 years of age. Do not use on babies and children.
Your scalp is red, inflamed, infected, irritated, or painful.
You use other medicines on the scalp.

OTC - WHEN USING SECTION

Avoid contact with eyes. In case of accidental contact, rinse eyes with a large amount of cool tap water.

OTC - STOP USE SECTION

·Chest pain, rapid heartbeat, faintness, or dizziness occurs
·Sudden, unexplained weight gain occurs.
. Scalp irritation or redness occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

DOSAGE & ADMINISTRATION SECTION


Please familiarize yourself with the instructions below in order to help make your product application a success.
This product should be used twice daily, every day.
To be effective, it is important to apply the product directly to your scalp and not to your hair so that it can easily get to your hair follicles to help regrow your hair.
There is no need to shampoo your hair before using the product.

INACTIVE INGREDIENT SECTION

Butylene Glycol
Glycerin
Alcohol
Panthenol
Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label2label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311724minoxidil 5 % Topical SolutionPSN1
311724minoxidil 50 MG/ML Topical SolutionSCD1
311724minoxidil 3 GM per 60 ML Topical SolutionSY1
311724minoxidil 5 % Topical SolutionSY1
311724minoxidil 5 GM per 100 ML Topical SolutionSY1

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
83766-002-01RHRTTUE 5% Minoxidil Applicator Pens30 mL in 1 BOTTLE, WITH APPLICATORLIQUID301
83766-002-01RHRTTUE 5% Minoxidil Applicator Pens6 in 1 PACKAGELIQUID61

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
83766-00283766-002-01

Ingredients#

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

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

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
4f68ee3f-1471-1322-e063-6294a90a9e5a4f68ee3f-1470-1322-e063-6294a90a9e5a2026-04-14WarningsExact identifier
spl id: 4f68ee3f-1471-1322-e063-6294a90a9e5a
spl set id: 4f68ee3f-1470-1322-e063-6294a90a9e5a

Reported adverse events (FAERS/openFDA)#

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