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Johnson Foam Pro Finasteride Foam with 5% Minoxidil .25 g/100g; 5 g/100g Aerosol, Foam, 90 g — NDC 84539-0002-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Johnson Foam Pro Finasteride Foam with 5% Minoxidil .25 g/100g; 5 g/100g Aerosol, Foam, 90 g — NDC 84539-002-01 (Billing 84539-0002-01)

by JOHNSON BIOPHARMACEUTICAL INC. · 90 g in 1 BOTTLE

This is a package of 90 g of Johnson Foam Pro Finasteride Foam with 5% Minoxidil .25 g/100g; 5 g/100g Aerosol, Foam from JOHNSON BIOPHARMACEUTICAL INC., marketed since Nov 2024 and currently FDA-listed. It is this product's only package size.

NDC 84539-0002-01
🏷️ FDA NDC (as labeled) 84539-002-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Aug 6, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 84539-002-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84539 labeler · 002 product · 01 package
Package marketed since
Nov 21, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8453900201 9
FDA record last changed
Aug 6, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84539-002-01
Product NDC 84539-002
11-digit billing NDC 84539000201
UNII 57GNO57U7G, 5965120SH1
Application # 505G(a)(3)
SPL Set ID 27697b1c-f713-f7e0-e063-6394a90a7514
Established class (EPC) 5-alpha Reductase Inhibitor; Arteriolar Vasodilator
Mechanism of action 5-alpha Reductase Inhibitors
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 2024-11-21
Route TOPICAL
Dosage form AEROSOL, FOAM
Substance FINASTERIDE; MINOXIDIL
Why two NDCs? The FDA registers this code as 84539-002-01 — 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 → 84539-0002-01. 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.

Clinical

🧪 What is this product?

Johnson Foam Pro is a topical foam aerosol containing finasteride and minoxidil, marketed as an over-the-counter monograph product. Finasteride is a 5-alpha reductase inhibitor typically used to address hair loss, while minoxidil functions as an arteriolar vasodilator commonly applied topically for the same purpose. The two active ingredients work through different mechanisms and are both commonly found in products designed to address male pattern baldness.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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.

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.
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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
84539-0002-01 You're viewing this Main listing 90 g in 1 BOTTLE 2024-11-21 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Johnson Foam Pro .25 g/100g; 5 g/100gthis 84539-0002-01 JOHNSON 90 g — — 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

🏛️
2024
On the market since
Nov 2024
📍
2026
Currently FDA-listed
2 years 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.

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 1P9D0Z171K
    BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
  • UNII 035JKJ76MT
    A silicone-based ingredient that helps oil and water mix together in formulations. It works as an emulsifier to create smooth, stable textures in topical medicines and creams.
  • UNII 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life 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 BZ1R15MTK7
    Levomenthol is the left-handed form of menthol, a natural cooling compound from mint plants. It's used in medicines as a flavoring agent and to provide a cooling sensation on the skin or mucous membranes.
  • UNII TUF2IVW3M2
    Poloxamer 407 is a synthetic polymer made from ethylene oxide and propylene oxide. In medicines, it acts as a thickener, emulsifier, and solubilizer to help mix ingredients and create the right texture.
  • UNII 6OZP39ZG8H
    Polysorbate 80 is a synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together in medications and improves how the product disperses in the body.
  • UNII M9NL0C577Y
    Ubiquinol is a fat-soluble compound found naturally in cells that acts as an antioxidant. In medicines, it serves as an active nutritional ingredient to support formulation stability and bioavailability.
  • 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.
  • UNII C32PQ86DH4
    Zinc PCA is a zinc salt of pyroglutamic acid, a naturally occurring amino acid derivative. It's used in medications as a skin-conditioning agent and to help maintain product stability and texture in topical formulations.

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

The official label also statesALCOHOL GLYCERIN WHATER CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) UBIQUINOL ZINC PIDOLATE BUTYLATED HYDROXYTOLUENE EDETATE DISODIUM LEVOMENTHOL Poloxzam POLYSORBATE 80

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 DailyMed — ingredient 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.

Manufacturer & labeler

LabelerJOHNSON BIOPHARMACEUTICAL INC.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code84539
First marketedNov 2024
Product typeHuman Otc Drug
Portfolio2 products on file

More NDCs from JOHNSON BIOPHARMACEUTICAL INC. labeler code 84539

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.

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 ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 7 words ▾

Fight primarycause ofhalr loss in men.Antihalrlosstohelpincreasehairdenslty andvolume.

⏱️ Dosage and Administration 90 words ▾

1.PREP HANDSWITH COLD WATERRinse Your Fingers inCald WaterAnd Doy Them note: Foam Wll MeltOn Contat WithWarmSurfacs. 2.OPENCHILD RESISTANTCAPBe Sure To Align Arrow On The CapWith Arrow On Blue Ring.Tit capBadkAnd Pull ot. 3.DISPENSEVERTICALLYONTOACOLDSURFACEHoldThe Can Staght UpsideDown.if You Hdd ThecanAtAnAngle, Foam May Nat DispansePoperhy, PressNozzie To Dispe nseHalfACapiu OfFoam Onto CaldSuface(e gdshorCod Hands).

4.APPLYTOSCALP, NOTHAIRPart Your Hair To Expose HairLossAra. Massage Foamhno Sedp.NotHair, Repeat UnslAllHar LossAras Have Been Covered. 5.CLOSE CAP AND WASHHANDSsn ap cap back into plaoe be surearows do notline up,socapmmanschid resistant, wash hands andamysurace thoroughly a feruse .

⚠️ Warnings 17 words ▾

Forexternaluse only. Foruse by men only. Extremely Flammable. Avoid fire, flame, or smoking during andimmedlately following application.

🧪 Active Ingredient 4 words ▾

MINOXIDIL 5% FINASTERIDE 0.25%

🧪 Inactive Ingredients 19 words ▾

ALCOHOL GLYCERIN WHATER CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) UBIQUINOL ZINC PIDOLATE BUTYLATED HYDROXYTOLUENE EDETATE DISODIUM LEVOMENTHOL Poloxzam POLYSORBATE 80

🎯 Purpose 7 words ▾

Fight primarycause ofhalr loss in men.Antihalrlosstohelpincreasehairdenslty andvolume.

📄 Do Not Use 48 words ▾

you have no famlly hlstory of halrloss. you rhalrloss is sudden and/or patchy. you do not know the reason for your halr loss. you are under 18 years of age. Do not useonbables or chikdren. yourscalp is red, inflamed,infected,rritated, or painful. you use other medicines on the scalp.

📄 When Using This Product 31 words ▾

do not apply on other parts of the body. avold contact with eyes. In case ofaccldental contact.rinse eyes with large amounts ofcooltap water. some people have experienced changes in halr colorandortexture.

📄 Stop Use and Ask a Doctor If 29 words ▾

chest pain, rapld heartbeat, faintness,ordlzziness occurs. sudden,unexplained weight gain occurs. your hands or feet swell. scalp irritation or redness occurs. umwanted facialhalrgrowth occurs. you donot see halrregrowthin 4 months.

📄 Keep Out of Reach of Children 10 words ▾

If swallowed,getmedical help or contacta Poison Control Center right away.

📄 Package Label / Principal Display Panel 1 words ▾

label3

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 JOHNSON BIOPHARMACEUTICAL INC.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
JOHNSON BIOPHARMACEUTICAL INC. 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.
← 84539-0001-01 · JOHNSON 84540-0130-01 · NPG →
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.