Home › NDC Lookup › Ingredients › Minoxidil 5% › 85304-0002-01
5% Minoxidil Hair Growth Sprays Serum 5 g/100mL; .5 g/100mL Liquid — NDC 85304-0002-01 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 Sprays Serum 5 g/100mL; .5 g/100mL Liquid — NDC 85304-002-01 (Billing 85304-0002-01)

by Guangzhou Borderless Technology Co., Ltd. · 3 BOTTLE in 1 PACKAGE / 100 mL in 1 BOTTLE

This is a package of 5% Minoxidil Hair Growth Sprays Serum 5 g/100mL; .5 g/100mL Liquid from Guangzhou Borderless Technology Co., Ltd., marketed since Apr 2025 and currently FDA-listed. It is this product's only package size.

NDC 85304-0002-01
🏷️ FDA NDC (as labeled) 85304-002-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 27, 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 85304-002-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
85304 labeler · 002 product · 01 package
Package marketed since
Apr 27, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8530400201 2
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85304-002-01
Product NDC 85304-002
11-digit billing NDC 85304000201
RxCUI 2715603
UNII 5965120SH1, 6SO6U10H04
Application # 505G(a)(3)
SPL Set ID 33bd946d-1815-b60b-e063-6294a90a63c1
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 2025-04-27
Route TOPICAL
Dosage form LIQUID
Substance MINOXIDIL; BIOTIN
Quick answers
  • RxCUI (RxNorm): 2715603
Why two NDCs? The FDA registers this code as 85304-002-01 — 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 → 85304-0002-01. 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.

RxNorm drug class

This medicine belongs to the Other plain vitamin preparations class.

Drug family (ATC) Other plain vitamin preparations
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 is this product?

This is a topical liquid spray serum containing minoxidil and biotin, marketed as an over-the-counter monograph product. Minoxidil is typically used in hair-growth products to help stimulate hair follicles on the scalp. Biotin is a B vitamin commonly included in hair and nail supplements to support keratin production. The product is applied directly to the skin as a spray or serum formulation.

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
85304-0002-01 You're viewing this Main listing 3 BOTTLE in 1 PACKAGE / 100 mL in 1 BOTTLE 2025-04-27 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
5% Minoxidil Hair Growth Sprays Serum .005 g/mL; .05 g/mL 83766-0003-01 Shenzhen 7 bottles — — FDA listed —
5% Minoxidil Hair Growth Sprays Serum .005 g/mL; .05 g/mL 83766-0004-01 Shenzhen 8 bottles — — Discontinued —
5% Minoxidil Hair Growth Sprays Serum 5 g/100mL; .5 g/100mLthis 85304-0002-01 Guangzhou 3 bottles — — FDA listed —
Kweqdsd 5% Minoxidil Hair Growth Sprays Serum 5 g/100mL; .5 g/100mL 85304-0003-01 Guangzhou 3 bottles — — FDA listed —
FRNOIP 5% Minoxidil Hair Growth Sprays Serum 5 g/100mL; .5 g/100mL 85304-0004-01 Guangzhou 5 bottles — — FDA listed —
AMRWRIR 5% Minoxidil Hair Growth Sprays Serum 5 g/100mL; .5 g/100mL 85304-0005-01 Guangzhou 6 bottles — — FDA listed —
BLIYEOGZ 5% Minoxidil Hair Growth Sprays Serum .5 g/100mL; 5 g/100mL 85304-0006-01 Guangzhou 3 bottles — — FDA listed —
Sidinox 5% Minoxidil Hair Growth Sprays Serum .5 g/100mL; 5 g/100mL 85304-0007-01 Guangzhou 4 bottles — — FDA listed —
OCVWJKD 5% Minoxidil Hair Growth Sprays Serum .5 g/100mL; 5 g/100mL 85304-0008-01 Guangzhou 7 bottles — — FDA listed —
CYPKEB 5% Minoxidil Hair Growth Sprays Serum .5 g/100mL; 5 g/100mL 85304-0009-01 Guangzhou 4 bottles — — FDA listed —
Trzsfr 5% Minoxidil Hair Growth Sprays Serum .5 g/100mL; 5 g/100mL 85304-0011-01 Guangzhou 4 bottles — — FDA listed —
EZBIORT 5% Minoxidil Hair Growth Sprays Serum .5 g/100mL; 5 g/100mL 85304-0012-01 Guangzhou 4 bottles — — FDA listed —
TAGOQHA 5% Minoxidil Hair Growth Sprays Serum 5 g/100mL; .5 g/100mL 85304-0013-01 Guangzhou 3 bottles — — FDA listed —
ERWCNMIE 5% Minoxidil Hair Growth Sprays Serum 5 g/100mL; .5 g/100mL 85304-0014-01 Guangzhou 7 bottles — — FDA listed —
TNEGHC 5% Minoxidil Hair Growth Sprays Serum 5 g/100mL; .5 g/100mL 85304-0022-01 Guangzhou 5 bottles — — FDA listed —
AGIKENB 5% minoxidil with biotin topical solution .005 g/mL; .05 g/mL 85304-0029-01 Guangzhou 4 bottles — — FDA listed —
ONIADBA 5% Minoxidil Hair Growth Sprays Serum .05 g/mL; .005 g/mL 85992-0001-01 Shenzhen 4 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

🏛️
2025
On the market since
Apr 2025
📍
2026
Currently FDA-listed
1 year listed
🔒
·
Generic approved (availability unconfirmed)
see note
🔒Generic approved by FDA, but pharmacy availability is not confirmed

The FDA lists approved generic versions of this medicine, but that does not always mean a pharmacy can get one today. Patent rules, launch agreements, supply and pricing can affect when generics actually arrive.

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 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII D5340Y2I9G
    Castor oil is a natural plant-based oil used in medicines as a lubricant, laxative agent, and solvent. It helps medicine ingredients dissolve or flow smoothly and can aid bowel movement in formulations designed for that purpose.
  • UNII 1O6C93RI7Z
    Dexpanthenol is a naturally derived compound related to B vitamins. It acts as a humectant and skin conditioning agent, helping the medicine absorb moisture and maintain softness in topical formulations.
  • 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 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.

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

The official label also statesButylene Glycol Glycerin Alcohol Castor oil Dexpanthenol 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

LabelerGuangzhou Borderless Technology Co., Ltd.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code85304
First marketedApr 2025
Product typeHuman Otc Drug
Portfolio33 products on file

More NDCs from Guangzhou Borderless Technology Co., Ltd. labeler code 85304

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 6 words ▾

Use to regrow hair and beard

⏱️ Dosage and Administration 56 words ▾

1.Make sure your hair and scalp are dry(no need to wash your hair before each use). 2.Apply 3-4 pumps of spray directly to the treated area of the scalp. 3.Gently massage into the scalp or thinning hair areas until absorbed. 4.Continued use is required to increase and maintain hair regrowth, Discontinuation may lead to hair loss

⚠️ Warnings 10 words ▾

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

🧪 Active Ingredient 4 words ▾

Minoxidil 5% Biotin 0.5%

🧪 Inactive Ingredients 8 words ▾

Butylene Glycol Glycerin Alcohol Castor oil Dexpanthenol Water

🎯 Purpose 3 words ▾

Hair Regrowth Treatment

📄 Do Not Use 54 words ▾

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.

📄 When Using This Product 92 words ▾

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 andlor texture.

It takes time to regrow hair, Results may occur at 3 months with twice a day usage. For some men, youmay need to use this product for at least 6 months before you see results, The amount of hair regrowth isdifferent for each person. Avoid contact with eyes.

In case of accidental contact, rinse eyes with a large amount of cool tap water.

📄 Stop Use and Ask a Doctor If 30 words ▾

Chest pain, rapid heartbeat, faintness, or dizziness occurs. Sudden, unexplained weight gain occurs. If unwanted facial hair growth occurs . If you do not see hair regrowth in 6 months.

📄 Keep Out of Reach of Children 18 words ▾

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

📄 Package Label / Principal Display Panel 1 words ▾

label1

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 Guangzhou Borderless Technology Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangzhou Borderless 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.
← 85304-0001-02 · Guangzhou 85304-0003-01 · Guangzhou →
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.