Over-the-counter drug · OTC MONOGRAPH DRUG
Minoxidil Hair Growth Serum (Minoxidil) NDC 85741-004
Minoxidil 5 g/100mL · Liquid · Topical · Shenzhen Deshijian Medical Equipment Co., Ltd
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 85741-004-01 | 8574100040185741000401 | 1 BOTTLE in 1 BOX (85741-004-01) / 60 mL in 1 BOTTLEMarketed from Jun 4, 2026 | |
| 85741-004-02 | 8574100040285741000402 | 3 BOX in 1 BAG (85741-004-02) / 1 BOTTLE in 1 BOX / 60 mL in 1 BOTTLEMarketed from Jun 4, 2026 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Minoxidil Hair Growth Serum
- Generic name (nonproprietary)
- minoxidil
- Active ingredients
- Minoxidil — 5 g/100mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- Shenzhen Deshijian Medical Equipment Co., LtdNDC labeler code 85741
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 032
- Marketing start
- Listing expires
- Other FDA classes
- Arteriolar Vasodilation (Physiologic effect)
- Identifiers
- Product ID 85741-004_53796d44-0ad2-fe13-e063-6394a90a122eSPL ID 53796d44-0ad2-fe13-e063-6394a90a122eSPL set ID 535cdf78-90bc-86b4-e063-6294a90a2c20RxCUI 311724UNII 5965120SH1
- Pharmacologic class
- Arteriolar Vasodilator
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N485741000401followed by a unit qualifier and the quantityPackage 85741-0004-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
1.Apply 2-3 drops of the serum directly to the affected area of the scalp. 2.Massage into the scalp with your fingers, then wash your hands thoroughly. 3.Using more serum or applying it more frequently will not improve your results. 4.Continued use is necessary to promote and maintain hair regrowth. 5.Discontinuing use may lead to hair loss.
Excerpt only. Read the full label for complete information.
About NDC 85741-004
- What is NDC 85741-004?
- 85741-004 is the product NDC for Minoxidil Hair Growth Serum (minoxidil), Minoxidil 5 g/100mL liquid, listed with the FDA by Shenzhen Deshijian Medical Equipment Co., Ltd. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Minoxidil Hair Growth Serum (Minoxidil).
- What is the active ingredient?
- Minoxidil.
- Who is the labeler?
- Shenzhen Deshijian Medical Equipment Co., Ltd, NDC labeler code 85741. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Minoxidil Hair Growth Serum?
- 2 other product NDCs are listed under this name. See all Minoxidil Hair Growth Serum NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Minoxidil Hair Growth Serum products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Minoxidil Hair Growth Serumminoxidil | Minoxidil .5 g/10g | LiquidTopical | Guangzhou Ariel Medical Technology Co., Ltd. | 87815-001 | 87815-0001-0187815-0001-0287815-0001-03 |
| Minoxidil hair growth serum | Minoxidil 50 mg/100mL | LiquidTopical | Jiashen International Trade Limited | 84867-005 | 84867-0005-01 |
Other NDCs under M 032
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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