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Minoxidil Topical Solution USP, 2% .02 g/mL Solution — NDC 87532-0001-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Minoxidil Topical Solution USP, 2% .02 g/mL Solution — NDC 87532-001-01 (Billing 87532-0001-01)

by Carol's Daughter, LLC · 1 BOTTLE in 1 BOX / 60 mL in 1 BOTTLE

This is a package of Minoxidil Topical Solution USP, 2% .02 g/mL Solution from Carol's Daughter, LLC, marketed since Apr 2026 and currently FDA-listed. It is this product's only package size.

NDC 87532-0001-01
🏷️ FDA NDC (as labeled) 87532-001-01 billing pads the product segment with a zero
OTC Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87532-001-01
Product NDC 87532-001
11-digit billing NDC 87532000101
RxCUI 311723
UNII 5965120SH1
Application # ANDA078176
SPL Set ID 4d659f8f-b721-cf3b-e063-6394a90a50f6
Established class (EPC) Arteriolar Vasodilator
Physiologic effect Arteriolar Vasodilation
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-04-03
Route TOPICAL
Dosage form SOLUTION
Substance MINOXIDIL
Quick answers
  • RxCUI (RxNorm): 311723
Why two NDCs? The FDA registers this code as 87532-001-01 — 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 → 87532-0001-01. 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.

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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • The topical products in the label are specifically approved for hair regrowth on the top of the scalp only — not for use on other parts of the body. Applying it elsewhere isn't rec...
  • Can I use the topical minoxidil solution on my beard or other areas, not just my scalp?
  • Hair regrowth takes time and patience. Some people start to see results after about 2 months of twice-daily use, but for others it may take 4 months or more. Not everyone responds...
  • How long does it take to see results with topical minoxidil?
📖 Read our full Minoxidil guide →

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 mLPer 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
87532-0001-01 You're viewing this Main listing 1 BOTTLE in 1 BOX / 60 mL in 1 BOTTLE 2026-04-03 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Good Sense Hair Regrowth Treatment 2 g/100mL 00113-6500-00 L. 3 bottles — — FDA listed —
hair regrowth treatment 2 g/100mL 00363-0703-16 Walgreen 1 bottle — — FDA listed —
Minoxidil 2 g/100mL 00363-9970-02 Walgreens 1 bottle — — FDA listed —
up and up hair regrowth treatment for women 2 g/100mL 11673-0919-30 Target 3 bottles — — FDA listed —
carols daughter hair regrowth treatment 2 g/100mL 49967-0988-01 L'Oreal 1 bottle — — FDA listed —
Womens Minoxidil Hair Growth System 20 mg/mL 51326-0161-01 Topiderm, 60 ml — — FDA listed —
Minoxidil Topical Solution 2% 20 mg/mL 51672-2152-04 SUN 1 bottle — — FDA listed —
minoxidil 2 g/100mL 56062-0070-16 Publix 1 bottle — — FDA listed —
minoxidil topical 2 g/100mL 59640-0000-16 H 1 bottle — — FDA listed —
BOSLEY Woman 2 Minoxidil Topical Solution 20 mg/mL 69113-0432-00 Scientific 1 bottle — — FDA listed —
BOSLEY Minoxidil Topical Solution 2 for Women 20 mg/mL 69113-0462-00 Scientific 1 bottle — — FDA listed —
Foligain Professional Series Extra Strength for Women Minoxidil Topical Hair Regrowth Treatment 20 mg/mL 69607-9530-00 WR 3 bottles — — FDA listed —
hair regrowth treatment 2 g/100mL 69842-0797-16 CVS 1 bottle — — FDA listed —
Womens Rogaine Unscented 20 mg/mL 69968-0090-01 Kenvue 1 bottle — — FDA listed —
Leader minoxidil 2 g/100mL 70000-0728-01 Cardinal 3 bottles — — FDA listed —
Keranique 2% Hair Regrowth Treatment for Women 20 mg/mL 70550-0576-01 PROFECTUS 1 bottle — — FDA listed —
hers hair regrowth treatment 2 g/100mL 71730-0023-16 Hims 1 bottle — — FDA listed —
MDhair hair regrowth treatment for women 2 g/100mL 71804-0711-02 MDalgorithms, 1 bottle — — FDA listed —
basic care hair regrowth treatment 2 g/100mL 72288-0202-30 Amazon.com 3 bottles — — FDA listed —
basic care hair regrowth treatment 2 g/100mL 72288-0701-16 Amazon.com 1 bottle — — FDA listed —
Gemachlich ZuHause Hair Growth Serum (Women) 2 g/100mL 76986-0012-01 Guangdong 8 bottles — — FDA listed —
hair regrowth treatment 2 g/100mL 79481-0070-01 Meijer, 3 bottles — — FDA listed —
equate hair regrowth treatment 2 g/100mL 79903-0072-30 WALMART 3 bottles — — FDA listed —
Santo Remedio Womens Hair Regrowth Treatment Minoxidil Unscented 20 mg/mL 81352-0561-00 SANTO 1 bottle — — FDA listed —
Remixdil Hair Regrowth Treatment For Women 2 g/100mL 83004-0009-01 Rida 4 bottles — — FDA listed —
Hair Regen Hair Regrowth Treatment 2 g/100mL 84232-0004-01 YIWUYIZHOUTRADINGCO.,LTD 60 ml — — FDA listed —
GROWELL Womens Hair Regrowth Treatment 2 Minoxidil 20 mg/mL 84329-0466-00 APIRA 1 bottle — — FDA listed —
The Root Of Goodness Healthy Growth Hair Regrowth System For Women 3 Step System 84828-0569-00 Invest 1 kit — — FDA listed —
eSalon Hair Regrowth Treatment Womens Minoxidil 20 mg/mL 84856-0604-00 ESALON.COM, 1 bottle — — FDA listed —
Happy Head Womens Hair Regrowth Treatment 20 mg/mL 87117-0880-00 Happy 3 bottles — — FDA listed —
Womens MinoGrow Hair Regrowth Treatment Minoxidil 20 mg/mL 87387-0980-00 Minogro 1 bottle — — FDA listed —
Fete Health Hair Regrowth Treatment for Women 20 mg/mL 87412-0981-00 Honest 1 bottle — — FDA listed —
Minoxidil Topical Solution USP, 2% .02 g/mLthis 87532-0001-01 Carol's 1 bottle — — FDA listed —
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
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

🏛️
2026
On the market since
Apr 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

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 5Z492UNF9O
    A synthetic liquid derived from propylene glycol, used in medicines as a solvent and humectant to dissolve active ingredients and maintain moisture in the formulation.
  • 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.

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

The official label also statesalcohol, propylene glycol, 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 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

LabelerCarol's Daughter, LLC
Application holderPURE SOURCE LLC
FDA applicationANDA078176 (ANDA)
Labeler code87532
First marketedApr 2026
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.

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 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 7 words ▾

Use to regrow hair on the scalp

⏱️ Dosage and Administration 48 words ▾

Directions • apply one mL with dropper 2 times a day directly onto the scalp in the hair loss area • using more or more often will not improve results • continued use is necessary to increase and keep your hair regrowth, or hair loss will begin again

⚠️ Warnings ~1 min read ▾

Warnings For external use only Flammable: Keep away from flame Do not use if • your degree of hair loss is different than that shown on the side of this carton, because this product may not work for you • 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 Ask a doctor before use if you have heart disease When using this product • do not apply on other parts of the body • avoid contact with the eyes.

In case of accidental contact, rinse eyes with large amounts of cool tap water • some people have experienced changes in hair color and/or texture • it takes time to regrow hair. You may need to use this product 2 times a day for at least 4 months before you see results • the amount of hair regrowth is different for each person. This product will not work for everyone Stop use and ask a doctor if • chest pain, rapid heartbeat, faintness, or dizziness occurs • sudden, unexplained weight gain occurs • your hands or feet swell • scalp irritation or redness occurs • unwanted facial hair growth occurs • you do not see hair regrowth in 4 months.

May be harmful if used when pregnant or breastfeeding. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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

🧪 Active Ingredient 5 words ▾

Active Ingredient Minoxidil 2% w/v

🧪 Inactive Ingredients 7 words ▾

Inactive ingredients alcohol, propylene glycol, purified water

🎯 Purpose 4 words ▾

Purpose Hair growth treatment

📄 Do Not Use 98 words ▾

Do not use if • your degree of hair loss is different than that shown on the side of this carton, because this product may not work for you • 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

📄 Ask a Doctor Before Use If 10 words ▾

Ask a doctor before use if you have heart disease

📄 When Using This Product 90 words ▾

When using this product • do not apply on other parts of the body • avoid contact with the eyes. In case of accidental contact, rinse eyes with large amounts of cool tap water • some people have experienced changes in hair color and/or texture • it takes time to regrow hair. You may need to use this product 2 times a day for at least 4 months before you see results • the amount of hair regrowth is different for each person.

This product will not work for everyone

📄 Stop Use and Ask a Doctor If 50 words ▾

Stop use and ask a doctor if • chest pain, rapid heartbeat, faintness, or dizziness occurs • sudden, unexplained weight gain occurs • your hands or feet swell • scalp irritation or redness occurs • unwanted facial hair growth occurs • you do not see hair regrowth in 4 months.

🤰 If Pregnant or Breast-Feeding 29 words ▾

May be harmful if used when pregnant or breastfeeding. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

📄 Keep Out of Reach of Children 20 words ▾

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

📄 Other Information 126 words ▾

Other information • see hair loss pictures on side of this carton • before use, read all information on carton and enclosed leaflet • keep the carton. It contains important information. • in clinical studies of mostly white women aged 18–45 years with mild to moderate degrees of hair loss, the following response to minoxidil topical solution 2% was reported: 19% of women reported moderate regrowth after using minoxidil topical solution 2% for 8 months (19% had moderate regrowth; 40% had minimal regrowth) this compares with 7% of women reporting moderate hair regrowth after using the placebo, the liquid without minoxidil in it, for 8 months (7% had moderate regrowth; 33% had minimal regrowth) • store at 20° to 25°C (68° to 77°F).

Keep tightly closed.

📄 Questions or Comments 4 words ▾

Questions or comments 1-877-540-2101

📄 Package Label / Principal Display Panel 2 words ▾

Minoxidil label

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

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 Carol's Daughter, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Carol's Daughter, LLC 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.
← 87528-0001-10 · VICI 87533-0332-01 · Ganzhou →
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.