apgwgzminoxidil2%
apgwgzminoxidil2% is an FDA drug label for the active ingredient MINOXIDIL manufactured by Guangdong Jiaoyu Biotechnology Co., Ltd administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260818.
- Generic name
- MINOXIDIL
- Manufacturer
- Guangdong Jiaoyu Biotechnology Co., Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87722-091
- Application
- M032
- Label effective
- 20260818
About this product
apgwgzminoxidil2% is an FDA-registered drug product whose active ingredient is MINOXIDIL. It is labelled by Guangdong Jiaoyu Biotechnology Co., Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87722-091, application M032, label effective 20260818. It is one of 90 FDA drug label records sharing the active ingredient MINOXIDIL. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing MINOXIDIL are most often described in connection with: helps regrow. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Indications & Usage
Helps regrow hair on the scalp
Dosage & Administration
Apply 1 mL directly to the scalp twice daily. Do not exceed the recommended dosage. More frequent use will not improve results. Continued use is necessary to maintain hair regrowth.
Warnings
For external use only. Do not use if your hair loss is sudden, patchy, or the cause is unknown; you are under 18 years of age; your scalp is red, inflamed, infected, irritated, or painful; or you use other medicines or treatments on the scalp. Ask a doctor before use if you have heart disease. When using this product, apply only to the scalp and avoid contact with eyes. Unwanted facial hair growth may occur. Changes in hair color or texture may occur. It may take 2–4 months to see results, and results vary by individual. Stop use and ask a doctor if chest pain, rapid heartbeat, dizziness, or fainting occurs; sudden weight gain or swelling occurs; severe scalp irritation occurs; or no hair growth occurs after 4 months of use.
More products with the same ingredient
MINOXIDIL5% Minoxidil Foam
View label5% Minoxidil Hair Growth Sprays Serum
View label5% Minoxidil Hair Growth Topical Solution
View label5% Minoxidil Hair Regrowth Serum With Biotin
View label5% Minoxidil Hair Regrowth Treatment
View label5% Minoxidil hair growth Serum
View label5% Minoxidil(For Men)
View label5%MINOXIDIL TOPICAL FOAM
View labelHow products containing MINOXIDIL compare
FDA lists 90 drug label records with MINOXIDIL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Bryant Ranch Prepack | 7 |
| — | — | Shenzhen Earth Surface Trading Co., Ltd. | 5 |
| — | — | Amazon.com Services LLC | 4 |
| — | — | Guangzhou Ariel Medical Technology Co., Ltd. | 4 |
| — | — | Guangzhou Jianyuan Biological Technology.Co.,Ltd | 4 |
Frequently asked questions
What is apgwgzminoxidil2% used for?
Helps regrow hair on the scalp
Who makes apgwgzminoxidil2%?
Guangdong Jiaoyu Biotechnology Co., Ltd is the labeler of record for apgwgzminoxidil2%. 90 FDA label records share the active ingredient MINOXIDIL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does apgwgzminoxidil2% come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is apgwgzminoxidil2% prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Are there other products containing MINOXIDIL?
Yes. 90 FDA drug label records list MINOXIDIL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has apgwgzminoxidil2% been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.