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5% Minoxidil Hair Growth Serum Roll-on Minoxidil 5% , Rosemary 1% .05 g/mL; .01 g/mL Liquid — NDC 85992-0007-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

5% Minoxidil Hair Growth Serum Roll-on Minoxidil 5% , Rosemary 1% .05 g/mL; .01 g/mL Liquid — NDC 85992-007-01 (Billing 85992-0007-01)

by Shenzhen Boyimei Technology Co., Ltd. · 3 BOTTLE in 1 BOX / 25 mL in 1 BOTTLE

This is a package of 5% Minoxidil Hair Growth Serum Roll-on Minoxidil 5% , Rosemary 1% .05 g/mL; .01 g/mL Liquid from Shenzhen Boyimei Technology Co., Ltd., marketed since Jul 2026 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 85992-0007-01
🏷️ FDA NDC (as labeled) 85992-007-01 billing pads the product segment with a zero
This package
Contains25 mL in 1 bottle Pack sizes2 compare ↓
Main listing for product 85992-007 · Also comes in: 4 bottles 85992-007-02
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 85992-007-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
85992 labeler · 007 product · 01 package
Package marketed since
Jul 31, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8599200701 6
FDA record last changed
Aug 6, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85992-007-01
Product NDC 85992-007
11-digit billing NDC 85992000701
UNII 5965120SH1, IJ67X351P9
Application # 505G(a)(3)
SPL Set ID 57e4ccae-7989-a36e-e063-6394a90a9927
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 2026-07-31
Route TOPICAL
Dosage form LIQUID
Substance MINOXIDIL; ROSEMARY
Why two NDCs? The FDA registers this code as 85992-007-01 — 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 → 85992-0007-01. 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?

This is a topical liquid hair growth serum sold as an over-the-counter monograph product. The main active ingredient, minoxidil, is typically used to promote hair growth and is applied directly to the scalp. Rosemary extract is included as a supporting botanical ingredient commonly found in hair care products. The product comes in a roll-on applicator format for topical application to affected areas of the scalp.

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.
Try another pack size: 4 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
85992-0007-01 You're viewing this Main listing 3 BOTTLE in 1 BOX / 25 mL in 1 BOTTLE 2026-07-31 — Active
85992-0007-02 85992-007-02 4 BOTTLE in 1 BOX / 25 mL in 1 BOTTLE 2026-07-31 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 3 bottle in 1 box / 25 ml in 1 bottle.
What NDC number is used to bill for this package of 5% Minoxidil Hair Growth Serum Roll-on Minoxidil 5% , Rosemary 1% .05 g/mL; .01 g/mL Liquid?
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
5% Minoxidil Hair Growth Serum Roll-on .05 g/mL; .01 g/mLthis 85992-0007-01 Shenzhen 3 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

🏛️
2026
On the market since
Jul 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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 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 6SO6U10H04
    Biotin is a B-vitamin used as a nutritional supplement in some medications. It may also serve as a colorant or marker in formulations.
  • UNII TMS4MGA0H4
    A synthetic liquid derived from petroleum-based chemistry. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in topical or liquid formulations.
  • UNII 19F5HK2737
    Pantothenic acid is a B vitamin used in some formulations as a nutritional supplement or to support stability. It may also serve as a buffer or pH adjuster in the medicine.
  • UNII W4X7H8GYFM
    Polyethylene glycol (PEA) is a synthetic polymer derived from petroleum. It functions as a solvent, lubricant, and binder in medications to improve texture, reduce sticking, and help bind ingredients together.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII 6BJQ43T1I9
    A synthetic peptide made from copper and amino acids. It's used in topical formulations as an active conditioning or skin-support ingredient, though classified as an excipient in some product listings.
  • UNII L9153EKV2Y
    Red clover is a plant-derived ingredient used as a natural colorant and flavoring agent in medicines. It may also serve as a filler to add bulk to tablets or capsules.
  • UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • UNII 1NT28V9397
    Thuja occidentalis is a plant extract from the evergreen arborvitae tree. It's used in some formulations as a flavoring agent or botanical ingredient.
  • UNII CO450M8A6J
    A plant material derived from the whole mung bean plant. It functions as a filler and binder to give the tablet or capsule its structure and help hold ingredients together.

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

The official label also statesAqua,Butanediol,Biotin,Redensyl, Anagain, Arborvitae Leaf Extract, Vigna Radiata, Red Clover, Sorbic Acid Potassium Salt, Sodium Hyaluronate, Pantothenic Acid, Copper Peptide.

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

LabelerShenzhen Boyimei Technology Co., Ltd.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code85992
First marketedJul 2026
Product typeHuman Otc Drug
Portfolio7 products on file

More NDCs from Shenzhen Boyimei Technology Co., Ltd. labeler code 85992

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 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 30 words ▾

1.Naturally activate hair follicles and promote hair regrowth. 2.Extend the hair growth cycle,enhance hair resilience, and effectively reduce hair loss. 3.Balance scalp sebum secretion and optimize the scalp tissue microenvironment.

⏱️ Dosage and Administration 69 words ▾

Step 1: Ensure that your hair and scalp are dry and free of excess oil. Step 2: On areas with hair loss or thinning, gently press the roller ball tip onto the scalp and roll slowly for precise application. Follow the graduation mark on the bottle -each use is 1 ml. For best results, use consistently to boost and maintain hair regrowth.​Stopping treatment may lead to hair loss returning

⚠️ Warnings 10 words ▾

Keep out of reach of children. For external use only.

🧪 Active Ingredient 4 words ▾

Minoxidil 5% Rosemary 1%

🧪 Inactive Ingredients 19 words ▾

Aqua,Butanediol,Biotin,Redensyl, Anagain, Arborvitae Leaf Extract, Vigna Radiata, Red Clover, Sorbic Acid Potassium Salt, Sodium Hyaluronate, Pantothenic Acid, Copper Peptide.

🎯 Purpose 3 words ▾

Hair Regrowth Treatment

📄 Do Not Use 54 words ▾

Your hair loss is sudden 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

📄 When Using This Product 74 words ▾

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, youmay need to use this product for at least 4 months before you see results. The amount of hair regrowth isdifferent for each person. Avoid contact with eyes. In case of accidental contact, rinse your eyes with a large amount of cool tap water.

📄 Keep Out of Reach of Children 18 words ▾

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

📄 Package Label / Principal Display Panel 2 words ▾

label 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

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 Shenzhen Boyimei 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 1 other package presentation of this same product, including 4 bottles (85992-0007-02). 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 Boyimei 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.
← 85992-0006-01 · Shenzhen 85996-0001-01 · Totally →
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.