5% Minoxidil Hair Care Solution

Manufacturer
Shenzhen Linglong Trading Co., Ltd.
Effective date
2026-01-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:34:46

Label at a glance#

Product5% Minoxidil Hair Care Solution
Active ingredientMINOXIDIL
Label structure12 sections

Dosage and administration

This product cannot replace medicine and is only used for scalp and hair care

Storage and handling

Store in a sealed, cool and dry place, away from direct sunlight, and the temperature should not exceed 30℃

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Minoxdli 5% w/w

Purpose

OTC - PURPOSE SECTION

Hair regrowh Teotnent

Use

INDICATIONS & USAGE SECTION

Use to regrow hair on the scalp

Warnings

WARNINGS SECTION

Flammable. Keep away from fire sources or flames. For extemal use only

Do not use

OTC - DO NOT USE SECTION

You have no family history of hair loss
Your hair loss is sudden or patchy
Your hair loss is related to childbirth
You still don't know the cause of hair loss
You are under 18 years old. Do not use on infants and children
Your scalp is red, inflamed, infected or painful
You are currently using other medications on your scalp

OTC - WHEN USING SECTION

In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

1. This product is contraindicated for those allergic to minoxidil, ethanol, propylene glycol and other
components. It is recommended to conduct a local skin test for the first use
2. If any discomfort such as redness, swelling, itching or rash occurs during use, stop using it immediately and
consult a doctor

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

This product cannot replace medicine and is only used for scalp and hair care

Other information

STORAGE AND HANDLING SECTION

Store in a sealed, cool and dry place, away from
direct sunlight, and the temperature should not
exceed 30℃

Inactive ingredients

INACTIVE INGREDIENT SECTION

Batana oil, rosemary, purified water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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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
87376-001-015% Minoxidil Hair Care Solution60 mL in 1 BOTTLELIQUID601
87376-001-025% Minoxidil Hair Care Solution4 in 1 BOXLIQUID41

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
87376-00187376-001-01, 87376-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
5% Minoxidil Hair Care Solution5% MINOXIDIL HAIR CARE SOLUTIONShenzhen Linglong Trading Co., Ltd.49195e81-4a86-839b-e063-6294a90ac8832026-01-23WarningsExact identifier
ndc (package): 87376-001-01
ndc (package): 87376-001-02
ndc (product): 87376-001
ndc11 (package): 87376000101
ndc11 (package): 87376000102
spl id: 491962a9-ec6a-f292-e063-6294a90a3c03
spl set id: 49195e81-4a86-839b-e063-6294a90ac883

Reported adverse events (FAERS/openFDA)#

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