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GOOD SENSE HAIR REGROWTH TREATMENT Minoxidil 2 g/100mL Solution — NDC 00113-6500-00 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

GOOD SENSE HAIR REGROWTH TREATMENT Minoxidil 2 g/100mL Solution — NDC 0113-6500-00 (Billing 00113-6500-00)

by L. Perrigo Company · 3 BOTTLE in 1 CARTON / 60 mL in 1 BOTTLE

This is a package of GOOD SENSE HAIR REGROWTH TREATMENT Minoxidil 2 g/100mL Solution from L. Perrigo Company, marketed since Oct 2025 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 00113-6500-00
🏷️ FDA NDC (as labeled) 0113-6500-00 billing pads the labeler segment with a zero
This package
Contains60 mL in 1 bottle Pack sizes2 compare ↓
Main listing for product 0113-6500 · Also comes in: 3 bottles 0113-6500-30
OTC Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 20, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 0113-6500-00
Product NDC 0113-6500
11-digit billing NDC 00113650000
RxCUI 311723
UNII 5965120SH1
Application # ANDA075357
SPL Set ID b1bf381e-8f13-4a7e-a2f6-ba750d4d67e7
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 2025-10-24
Route TOPICAL
Dosage form SOLUTION
Substance MINOXIDIL
Quick answers
  • RxCUI (RxNorm): 311723
Why two NDCs? The FDA registers this code as 0113-6500-00 — a 4-4-2 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 labeler segment → 00113-6500-00. 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

📖 What it is MedlinePlus · NLM

Minoxidil is used with other medications to treat high blood pressure. It is in a class of medications called vasodilators. It works by relaxing the blood vessels so that blood can flow more easily through the body. High blood pressure is a common condition and when not treated, can cause damage to the brain, heart, blood vessels, kidneys and other parts of the body. Damage to these organs may cause heart disease, a heart attack, heart failure, stroke, kidney failure, loss of vision, and other problems. In addition to taking medication, making lifestyle changes will also help to control your b...

Read the full MedlinePlus article ↗
📗 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 →
1
Nutrient depletion considerations

Minoxidil may be associated with lower levels of 1 nutrient — worth a chat with your pharmacist, not a cause for alarm.

An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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.
Try another pack size: 3 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
00113-6500-00 You're viewing this Main listing 3 BOTTLE in 1 CARTON / 60 mL in 1 BOTTLE 2025-10-24 — Active
00113-6500-30 0113-6500-30 3 BOTTLE in 1 CARTON / 60 mL in 1 BOTTLE 2025-10-24 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 3 bottle in 1 carton / 60 ml in 1 bottle.
What NDC number is used to bill for this package of GOOD SENSE HAIR REGROWTH TREATMENT Minoxidil 2 g/100mL Solution?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Good Sense Hair Regrowth Treatment 2 g/100mLthis 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/mL 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

🏛️
2025
On the market since
Oct 2025
📍
2026
Currently FDA-listed
1 year listed
🔓
·
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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerL. Perrigo Company
Application holderL PERRIGO CO
FDA applicationANDA075357 (ANDA)
Labeler code00113
First marketedOct 2025
Product typeHuman Otc Drug
Portfolio228 products on file
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 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 fire or 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 breast-feeding. 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 regrowth 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 9 words ▾

May be harmful if used when pregnant or breast-feeding.

📄 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 127 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 hair 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? 1-800-719-9260

📄 Package Label / Principal Display Panel 58 words ▾

Package/Label Principal Display Panel GOODSENSE® Topical Solution Minoxidil Topical Solution USP, 2% Hair Regrowth Treatment For Women Clinically Proven to Help Regrow Hair Reactivates Hair Follicles to Stimulate Regrowth #1 Dermatologist Recommended Active Ingredient Three Month Supply Unscented Compare to active ingredient of Women’s Rogaine® 3-2 FL OZ (60 mL) BOTTLES TOTAL 6 FL OZ (180 mL) goodsense-hair-regrowth-treatment-carton-image.jpg

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

Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Minoxidil (matched by generic name) — the program that covers self-administered drugs. 3 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Minoxidil. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$3.5M
Claims incl. refills
260.9K
Beneficiaries
202.1K
Spend / beneficiary
$17.33
Spend / claim
$13.42
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

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) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 L. Perrigo Company. 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 1 other package presentation of this same product, including 3 bottles (00113-6500-30). 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?
L. Perrigo Company 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.
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.