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Olivita Extra Strength Minoxidil 50 mg/mL Solution — NDC 87695-008-00 (Billing 87695-0008-00)

by Olivita Beauty Inc · 1 BOTTLE, SPRAY in 1 BOX / 60 mL in 1 BOTTLE, SPRAY

This is a package of Olivita Extra Strength Minoxidil 50 mg/mL Solution from Olivita Beauty Inc, marketed since Aug 2026 and currently FDA-listed. It is this product's only package size.

NDC 87695-0008-00
🏷️ FDA NDC (as labeled) 87695-008-00 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 Sep 3, 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) 87695-008-00
Product NDC 87695-008
11-digit billing NDC 87695000800
RxCUI 311724
UNII 5965120SH1
Application # ANDA076239
SPL Set ID b2da549b-eb79-46ed-aaec-87326c4a1fbe
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 2026-08-06
Route TOPICAL
Dosage form SOLUTION
Substance MINOXIDIL
Quick answers
  • RxCUI (RxNorm): 311724
Why two NDCs? The FDA registers this code as 87695-008-00 — 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 → 87695-0008-00. 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

📗 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.

🧪 Full Minoxidil nutrient depletion report →
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.
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
87695-0008-00 You're viewing this Main listing 1 BOTTLE, SPRAY in 1 BOX / 60 mL in 1 BOTTLE, SPRAY 2026-08-06 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Regenpure Precision 50 mg/mL 71290-0813-02 Salonceuticals, 1 bottle — — FDA listed —
Minoxidil 50 mg/mL 00363-9971-02 Walgreens 1 bottle — — Discontinued —
BOSLEY Man 5 Minoxidil Topical Solution 50 mg/mL 69113-0431-00 Scientific 1 bottle — — FDA listed —
SUAVECITO 5% Minoxidil Solution 50 mg/mL 74866-0414-01 SUAVECITO, 1 bottle — — FDA listed —
INTELLIGENT Mens Minoxidil Extra Strength 5 Minoxidil 50 mg/mL 81632-0408-00 INTELLIGENT 1 bottle — — FDA listed —
Elevate Hair Regrowth Treatment 5 Minoxidil Solution 50 mg/mL 84561-0514-00 VAPOR 1 bottle — — FDA listed —
RegrowthX Hair Regrowth Treatment Minoxidil 50 mg/mL 87148-0881-00 Nimex 1 bottle — — FDA listed —
Foligain Professional Series Extra Strength For Men Minoxidil Hair Regrowth Treatment 50 mg/mL 69607-9540-00 WR 3 bottles — — FDA listed —
Minoxidil 50 mg/mL 00363-9973-06 Walgreens 3 bottles — — FDA listed —
Hair Regrowth Treatment Extra Strength for Men 50 mg/mL 82269-0607-02 Seiseidou 1 bottle — — Discontinued —
Nuvarra Mens Minoxidil Hair Regrowth Treatment 50 mg/mL 87779-0966-00 Bionetics 1 bottle — — FDA listed —
BOSLEY Minoxidil Topical Solution 5 (for men) 50 mg/mL 69113-0483-00 Scientific 1 bottle — — FDA listed —
DS Labs Spectral UHP Men s Extra Strength Hair Regrowth Treatment 50 mg/mL 69188-0593-00 DS 1 bottle — — FDA listed —
Mens Rogaine Extra Strength Unscented 50 mg/mL 69968-0089-01 Kenvue 1 bottle — — FDA listed —
Etaderm Mens Minoxidil Hair Regrowth Treatment Extra Strength 50 mg/mL 84180-0878-00 NUEPHASE 1 bottle — — FDA listed —
Elevate Hair Regrowth Treatment 5 50 mg/mL 84561-0524-00 VAPOR 1 bottle — — FDA listed —
Colorsmith Hair Regrowth Treatment Mens Minoxidil Topical Solution Extra Strength 50 mg/mL 84856-0603-00 ESALON.COM, 1 bottle — — FDA listed —
Mens Extra Strength Minoxidil Hair Growth Treatment 50 mg/mL 87616-0969-00 Hairmax 1 bottle — — FDA listed —
DAVV Minoxidil Topical Solution Mens Hair Regrowth Treatment 50 mg/mL 82372-0482-00 Good 1 bottle — — FDA listed —
Stafenit Hair Regrowth Treatment Topical Minoxidil 50 mg/mL 85097-0576-00 Cozesmo 1 bottle — — FDA listed —
ProBliva Mens Extra Strength Minoxidil 50 mg/mL 85464-0595-00 CAVTECH 1 bottle — — FDA listed —
RootVive Mens Hair Regrowth Treatment Extra Strength Minoxidil 50 mg/mL 87663-0962-00 TrueRoot 1 bottle — — FDA listed —
GROWELL Mens Hair Regrowth Treatment 5 Minoxidil 50 mg/mL 84329-0465-00 APIRA 1 bottle — — FDA listed —
Mens Jivexa Extra Strength Minoxidil 50 mg/mL 87688-0955-00 SMC 1 bottle — — FDA listed —
Santo Remedio Mens Hair Regrowth Treatment Minoxidil Topical Solution Extra Strength Unscented 50 mg/mL 81352-0560-00 SANTO 1 bottle — — FDA listed —
Tomum Hair Growth Treatment For Men Minoxidil Unscented 50 mg/mL 85003-0546-00 BELLEKA 1 bottle — — FDA listed —
Happy Head Mens Extra Strength Minoxidil 50 mg/mL 87117-0882-00 Happy 3 bottles — — FDA listed —
OpusMeds Extra Strength Minoxidil 50 mg/mL 87338-0983-00 Opus 1 bottle — — FDA listed —
Dr. Bosley Minoxidil (For Men) Hair Regrowth Treatment 50 mg/mL 69113-0913-00 Scientific 1 bottle — — FDA listed —
Follicly Minoxidil Hair Regrowth Treatment 50 mg/mL 87884-0006-00 Follicly 1 bottle — — FDA listed —
Olivita Extra Strength Minoxidil 50 mg/mLthis 87695-0008-00 Olivita 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
Aug 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.

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

LabelerOlivita Beauty Inc
Application holderPURE SOURCE LLC
FDA applicationANDA076239 (ANDA)
Labeler code87695
First marketedAug 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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 15 words ▾

Uses To regrow hair on the scalp (vertex only, see picture on side of carton)

⏱️ Dosage and Administration 75 words ▾

Directions • prime the sprayer by holding the bottle upright and pump the sprayer 5 times to ensure delivery of full spray Do not inhale mist • apply one ml with spray (6 sprays) 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. For use by men only. Flammable: Keep away from fire or flame Do not use • you are a woman. • your amount of hair loss is different than that shown on the side of this carton or your hair loss is on the front of the scalp.

5% minoxidil topical solution is not intended for frontal baldness or receding hairline. • you have no family history of hair loss. • your hair loss is sudden and/or patchy. • 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, irritated or painful. • you use other medicines on the scalp When Using • 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.

Results may occur at 2 months with twice a day usage. For some men, you may need to use this product 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 all men.

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.

Keep Out Of Reach Of Children

🧪 Active Ingredient 12 words ▾

Active Ingredient ** Minoxidil 5% w/v Purpose* Hair regrowth treatment for men

🧪 Inactive Ingredients 7 words ▾

Inactive ingredients Alcohol, Propylene Glycol, Purified Water

🎯 Purpose 6 words ▾

Purpose* Hair regrowth treatment for men

📄 Do Not Use 109 words ▾

Do not use • you are a woman. • your amount of hair loss is different than that shown on the side of this carton or your hair loss is on the front of the scalp. 5% minoxidil topical solution is not intended for frontal baldness or receding hairline. • you have no family history of hair loss. • your hair loss is sudden and/or patchy. • 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, irritated or painful. • you use other medicines on the scalp

📄 When Using This Product 99 words ▾

When Using • 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. Results may occur at 2 months with twice a day usage.

For some men, you may need to use this product 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 all men.

📄 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 25 words ▾

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

📄 Questions or Comments 10 words ▾

Questions or Comments? +1 (646) 736-4799 Visit Website at: www.olivitabeauty.com

📄 Package Label / Principal Display Panel 8 words ▾

Package Labeling: Outer Package Inner Package Insert Label

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.

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for MINOXIDIL — the ingredient across all brands.

Top reported reactions

Adverse Drug Reaction8,585
Alopecia3,803
Application Site Pruritus2,926
Overdose1,461
Application Site Irritation1,420
Application Site Pain1,413
Hair Texture Abnormal1,409

Age at onset

Neonate3
Infant14
Child18
Adolescent35
Adult4,531
Elderly2,902

Reporter sex

44,694 reports
Male · 58%
Female · 42%
Unknown · 0%

Serious outcomes

Death450
Disabling296
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 8,466 973
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

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 — Not published for this NDC No photo available yet for this listing.
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 Olivita Beauty Inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Olivita Beauty 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.
← 87693-0001-02 · SKIN 87697-0001-01 · Nanyang →
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.