Over-the-counter drug · OTC MONOGRAPH DRUG
Minoxidil Hair Regrowth Kit (Minoxidil) NDC 87813-001
Minoxidil .05 g/mL · Liquid · Topical · Guangzhou Zeus E-commerce Co., Ltd
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 87813-001-01 | 8781300010187813000101 | 4 BOTTLE in 1 BOX (87813-001-01) / 30 mL in 1 BOTTLEMarketed from Jun 25, 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 Regrowth Kit
- Generic name (nonproprietary)
- minoxidil
- Active ingredients
- Minoxidil — .05 g/mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- Guangzhou Zeus E-commerce Co., LtdNDC labeler code 87813
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Other FDA classes
- Arteriolar Vasodilation (Physiologic effect)
- Identifiers
- Product ID 87813-001_550bce76-4c79-80f0-e063-6394a90ad58fSPL ID 550bce76-4c79-80f0-e063-6394a90ad58fSPL set ID 550bce76-4c78-80f0-e063-6394a90ad58fRxCUI 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
N487813000101followed by a unit qualifier and the quantityPackage 87813-0001-01. 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)
Use to regrow hair of scalp and beard
Excerpt only. Read the full label for complete information.
About NDC 87813-001
- What is NDC 87813-001?
- 87813-001 is the product NDC for Minoxidil Hair Regrowth Kit (minoxidil), Minoxidil .05 g/mL liquid, listed with the FDA by Guangzhou Zeus E-commerce Co., Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Minoxidil Hair Regrowth Kit (Minoxidil).
- What is the active ingredient?
- Minoxidil.
- Who is the labeler?
- Guangzhou Zeus E-commerce Co., Ltd, NDC labeler code 87813. 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 Regrowth Kit?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Other NDCs under 505G(a)(3)
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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