HomeNDC LookupIngredientsMinoxidil 5% › 87086-0001-04
Carenice 5% Minoxidil HAIR REGROWTH TREATMENT 5 g/100g Aerosol, Foam — NDC 87086-0001-04 package photo

Carenice 5% Minoxidil HAIR REGROWTH TREATMENT 5 g/100g Aerosol, Foam

by Shenzhen Yifusi Technology Co., Ltd. · 4 BOTTLE in 1 PACKAGE (87086-001-04) / 60 g in 1 BOTTLE
NDC 87086-0001-04
🏷️ FDA NDC (as labeled) 87086-001-04 billing pads the product segment with a zero
This package
Contains60 g in 1 bottle Pack sizes5 compare ↓
OTC On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

🆔 Identity & classification

FDA NDC (as labeled) 87086-001-04
Product NDC 87086-001
11-digit billing NDC 87086000104
RxCUI 645146
UNII 5965120SH1
Application # 505G(a)(3)
SPL Set ID 3e4254d1-a0ce-a347-e063-6294a90a9d92
Established class (EPC) Arteriolar Vasodilator
Physiologic effect Arteriolar Vasodilation
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-09-08
Route TOPICAL
Dosage form AEROSOL, FOAM
Substance MINOXIDIL
Why two NDCs? The FDA registers this code as 87086-001-04 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 87086-0001-04. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏷️ RxNorm drug class

This medicine belongs to the Arteriolar Vasodilator class.

Pharmacologic class Arteriolar Vasodilator
Drug family (ATC) Pyrimidine derivatives, Other dermatologicals
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

🏭 Manufacturer & labeler

LabelerShenzhen Yifusi Technology Co., Ltd.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code87086
First marketedSep 2025
Product typeHuman Otc Drug
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

📗 Our plain-language guide HelloPharmacist
  • That's a really common question. Minoxidil tablets are very effective at lowering blood pressure, but they cause two side effects that need to be managed: your heart speeds up, and...
  • I've been prescribed minoxidil tablets for blood pressure — why do I need to take other pills with it?
  • It takes patience — most people need at least 2 to 4 months of twice-daily use before they notice any regrowth. Some products note that results can start appearing around the 2-mon...
  • I'm using a topical minoxidil solution for hair loss. How long before I see results?
📖 Read our full Minoxidil guide →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII 6LV4FOR43R
    Butane is a colorless gas derived from petroleum. In medicines, it serves as a propellant in inhalers and aerosol sprays, helping deliver the active drug to the lungs or skin.
  • UNII W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII BXR49TP611
    Isobutane is a liquefied gas used as a propellant in aerosol inhalers and sprays. It helps push the medicine out of the container so you can breathe or spray it as directed.
  • UNII 33X04XA5AT
    Lactic acid is a naturally occurring organic acid derived from milk or plant sources. It lowers and maintains pH in formulations, helps preserve the product, and can enhance ingredient stability and absorption.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 835370K47L
    A plant extract from the oriental arborvitae tree, used as a natural flavoring agent, fragrance component, or botanical additive in medicines to enhance taste or aroma.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII T75W9911L6
    A flammable gas used as a propellant in aerosol formulations. It helps dispense the medicine as a fine mist or spray when you activate the inhaler or pump.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII M6S840WXG5
    Purslane is a plant-derived ingredient used in pharmaceuticals as a natural source of beneficial compounds. It functions as an antioxidant and anti-inflammatory agent to help stabilize the formula and support product shelf life.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

15 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesInactive ingredients: isobutane, propane, alcohol, butane,glycerin, propyleneglycol, sttearic acid, cetearyl alcohol,polysorbate 20, lactic acid, phenoxyethanol, biota orientalis,leafextract, portulaca oleracea extract, purified water.

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMedingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer gPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 60 g 2 bottles 3 bottles 5 bottles
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Minoxidil 5% (For Men) 50 mg/g 51672-2128-04 Sun 1 can $0.300 Availability likely
Minoxidil For Women 50 mg/g 51672-2129-04 Sun 1 can $0.300 Availability likely
good sense hair regrowth treatment 5 g/100g 00113-0294-06 L. 6 cans Discontinued
Good Sense Hair Regrowth Treatment 50 mg/g 00113-1129-06 L. 6 cans FDA listed
minoxidil 50 mg/g 00113-5129-01 L. 60 g FDA listed
Good Sense Hair Regrowth Treatment 5 g/100g 00113-7080-01 L. 3 cans FDA listed
Minoxidil (For Men) 50 mg/g 00363-9090-01 Walgreen 1 can FDA listed
Minoxidil (For Women) 50 mg/g 00363-9091-01 Walgreen 1 can FDA listed
Minoxidil (For Men) 50 mg/g 11673-0157-03 TARGET 3 cans FDA listed
Minoxidil (For Women) 50 mg/g 11673-0158-04 TARGET 1 can FDA listed
Signature Care Hair Regrowth Treatment for men 5 g/100g 21130-0750-01 Safeway 60 g Discontinued
hair regrowth treatment for men 5 g/100g 30142-0294-01 Kroger 1 can Discontinued
hair regrowth treatment 50 mg/g 30142-0719-02 Kroger 2 cans Discontinued
hair regrowth treatment 5 g/100g 41250-0294-01 Meijer 1 can FDA listed
hair regrowth treatment 50 mg/g 41250-0749-01 Meijer 1 can FDA listed
equate hair regrowth treatment 5 g/100g 49035-0294-01 Wal-Mart 1 can FDA listed
equate hair regrowth treatment 50 mg/g 49035-0905-01 Wal-Mart 1 can FDA listed
Minoxidil (For Men) 50 mg/g 51316-0212-01 CVS 1 can Discontinued
Minoxidil (For Women) 50 mg/g 51316-0213-01 CVS 1 can Discontinued
Regoxidine (For Men) 50 mg/g 57483-0165-11 INNOVUS 1 can FDA listed
Regoxidine (For Women) 50 mg/g 57483-0175-11 INNOVUS 1 can FDA listed
Regoxidine (For Men) 50 mg/g 57483-0530-31 Innovus 3 cans FDA listed
Regoxidine (For Women) 50 mg/g 57483-0540-31 Innovus 2 cans FDA listed
Minoxidil 5% (For Women) 50 mg/g 58602-0607-01 Aurohealth 1 can FDA listed
Minoxidil 5% (For Men) 50 mg/g 58602-0608-01 Aurohealth 1 can FDA listed
Minoxidil 5% (For Men) 50 mg/g 59450-0210-01 Kroger 1 can FDA listed
Minoxidil (For Women) 50 mg/g 59450-0211-02 Kroger 2 cans FDA listed
Minoxidil 50 mg/g 59726-0115-60 P 60 g FDA listed
Minoxidil 50 mg/g 59726-0116-60 P 60 g FDA listed
Minoxidil 50 mg/g 59726-0122-60 P 1 can FDA listed
Minoxidil 50 mg/mL 59726-0125-60 P 1 can FDA listed
Minoxidil 50 mg/g 59726-0151-60 P 1 can FDA listed
hair regrowth treatment for men 5 g/100g 59779-0294-01 CVS 1 can Discontinued
kirkland signature Minoxidil 5 g/100g 63981-0294-06 Costco 6 cans FDA listed
members mark hair regrowth treatment 5 g/100g 68196-0469-04 Sam's 4 cans FDA listed
berkley and jensen minoxidil 5 g/100g 68391-0294-04 BJWC 4 cans FDA listed
Minoxidil (for Men) 50 mg/g 69113-0128-01 SCIENTIFIC 1 can FDA listed
Minoxidil (for Women) 50 mg/g 69113-0129-01 SCIENTIFIC 1 can FDA listed
Minoxidil For Men 50 mg/g 69113-0501-01 BosleyMD 1 can FDA listed
Minoxidil For Women 50 mg/g 69113-0502-01 BosleyMD 1 can FDA listed
hair regrowth treatment 50 mg/g 69842-0599-01 CVS 1 can Discontinued
Womens Rogaine Unscented 50 mg/g 69968-0030-01 Kenvue 1 can FDA listed
Mens rogaine Minoxidil Unscented Formula 50 mg/g 69968-0031-01 Kenvue 1 can FDA listed
Minoxidil For Women 50 mg/g 70000-0753-01 CARDINAL 1 can FDA listed
Minoxidil For Men 50 mg/g 70000-0754-01 CARDINAL 3 cans FDA listed
Minoxidil 50 mg/g 70550-0116-02 Keranique 1 can FDA listed
Minoxidil 5 Percent (For Women) 50 mg/g 70550-0605-04 PROFECTUS 1 can FDA listed
Minoxidil 5% (For Men) 50 mg/g 71713-0091-30 Thirty 3 cans FDA listed
keeps minoxidil topical 5 g/100g 71713-0092-30 THIRTY 3 cans FDA listed
Keeps Minoxidil Topical 5 g/100g 71713-0123-03 THIRTY 3 cans FDA listed
hers hair regrowth treatment 50 mg/g 71730-0129-01 Hims 1 can FDA listed
hims hair regrowth treatment 5 g/100g 71730-0294-01 Hims 1 can FDA listed
hims hair regrowth treatment 5 g/100g 71730-0700-01 Hims 1 can FDA listed
hers hair regrowth treatment 5 g/100g 71730-0813-01 Hims 1 can FDA listed
basic care hair regrowth treatment 50 mg/g 72288-0129-01 Amazon.com 1 can FDA listed
Basic Care Hair Regrowth Treatment 5 g/100g 72288-0294-03 Amazon.com 3 cans FDA listed
Gemachlich ZuHause Hair Growth Foam (Men) 5 g/100mL 76986-0008-01 Guangdong 60 ml FDA listed
Minoxidil (for Women) 50 mg/g 80855-0201-05 Virtue 1 can FDA listed
Hairfx Hair Growth Foam 5 g/100g 81653-0003-01 Guangzhou 60 g FDA listed
Hair regrowth treatment 5 g/100mL 81653-0005-01 Guangzhou 3 bottles FDA listed
Regenivade Hair Growth Foam 5 mg/mL 81653-0007-01 Guangzhou 1 bottle FDA listed
Minoxidil (For Men) 50 mg/g 82376-6006-03 SPAZI 3 cans FDA listed
Minoxidil (For Women) 50 mg/g 82376-6007-02 SPAZI 2 cans FDA listed
Minoxidil (for Men) 50 mg/g 82796-0100-01 RESTORATION 60 g FDA listed
Hair Growth Foam 5 g/100mL 83804-0008-01 Shenzhen 60 ml FDA listed
5% Minoxidil Hair Regrowth Foam 5 g/100g 84148-0025-01 Guangzhou 60 g FDA listed
Hair Regen - Hair Regrowth Treatment 5 g/100g 84232-0012-21 Yiwu 1 bottle FDA listed
Hair Regen - Hair Regrowth Treatment 5 g/100g 84232-0014-26 Yiwu 6 bottles FDA listed
Hair Regen - Hair Regrowth Treatment 5 g/100g 84232-0016-21 Yiwu 1 bottle FDA listed
Hair Regen - Hair Regrowth Treatment 5 g/100g 84232-0018-26 Yiwu 6 bottles FDA listed
Minoxidil 50 mg/g 84382-0001-04 Clarity 1 can FDA listed
Hair Beardgrowth Foam 5 g/100mL 85173-0001-01 Shenzhen 60 ml FDA listed
Minoxidil (For Men) 5 g/100g 85524-2611-02 FlexiGo 3 bottles FDA listed
Minoxidil (For Men) 5 g/100g 85524-2612-02 FlexiGo 1 bottle FDA listed
Gainxtra Hair Regrowth Treatment for Men and Women Minoxidil 5% Form with Biotin 50 mg/g 85929-0101-18 GAINXTRA 3 cans Discontinued
Carenice 5% Minoxidil HAIR REGROWTH TREATMENT 5 g/100gthis 87086-0001-04 Shenzhen 4 bottles FDA listed
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2025
On the market since
Sep 2025
📍
2026
Currently FDA-listed
1 year listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
87086-0001-01 1 BOTTLE in 1 PACKAGE (87086-001-01) / 60 g in 1 BOTTLE 2025-09-08 Active
87086-0001-02 2 BOTTLE in 1 PACKAGE (87086-001-02) / 60 g in 1 BOTTLE 2025-09-08 Active
87086-0001-03 3 BOTTLE in 1 PACKAGE (87086-001-03) / 60 g in 1 BOTTLE 2025-09-08 Active
87086-0001-04 You're viewing this 4 BOTTLE in 1 PACKAGE (87086-001-04) / 60 g in 1 BOTTLE 2025-09-08 Active
87086-0001-05 5 BOTTLE in 1 PACKAGE (87086-001-05) / 60 g in 1 BOTTLE 2025-09-08 Active

Pack size FAQ

What quantity is in NDC 87086-0001-04?
NDC 87086-0001-04 is listed by the FDA — 4 bottle in 1 package / 60 g in 1 bottle.
What NDC number is used to bill for this package of Carenice 5% Minoxidil HAIR REGROWTH TREATMENT 5 g/100g Aerosol, Foam?
Bill NDC 87086-0001-04 — the 11-digit billing format is 87086000104. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 87086-001-04, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 87086-0001-04, written without dashes as 87086000104. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 87086-0001-04, the first segment (87086) is the labeler code FDA assigned to Shenzhen Yifusi Technology Co., Ltd.; the middle segment (0001) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (04) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Shenzhen Yifusi Technology Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 4 other package presentations of this same product, including 1 bottle (87086-0001-01), 2 bottles (87086-0001-02), 3 bottles (87086-0001-03). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Shenzhen Yifusi Technology Co., Ltd. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage 16 words

Use to regrow hair on the top of the scalp(vertex only, see pictures on side carton)

⏱️ Dosage and Administration 134 words

1:PREP HANDSWITHCOLD WATER Rinse your fingers in cold water and dry them. Note: foam will melt oncontact with warmsurfaces. 2:OPEN THE CAP Hold the bottle with one hand and the lid with the other, then pull it open with force.

3:DISPENSE VERTICALLYONTO A COLD SURFACE Hold the can straight upside down. lf you hold the can at an angle, foam may not dispense properly.Press nozzle to dispense half a capful of foam onto cold surface (e.g. dish, or cold hands). 4: APPLY TO SCALPNOT HAIR Part your hair to expose hair loss area. Massage foam into scalp, not hair.Repeat until all hair loss areas have been covered.

5:CLOSE CAP ANDWASH HANDS Snap cap back into place.Be sure arrows do not line up, so cap remains child resistant.Wash hands and any surface thoroughly after use.

⚠️ Warnings 18 words

For external use only For use by men only Extremely Flammable:Avoid fire,flame,or smoking during and immediately following application.

🧪 Active Ingredient 2 words

MINOXIDIL 5%

🧪 Inactive Ingredients 23 words

Inactive ingredients : isobutane, propane, alcohol, butane,glycerin, propyleneglycol, sttearic acid, cetearyl alcohol,polysorbate 20, lactic acid, phenoxyethanol, biota orientalis,leafextract, portulaca oleracea extract, purified water.

🎯 Purpose 3 words

Hair regrowth treatment

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.