Over-the-counter drug · OTC MONOGRAPH DRUG
2% Minoxidil Serum For Women NDC 87593-103
Minoxidil 1 g/50g · Liquid · Cutaneous · Lance (Guangzhou) Biological Technology Co., Ltd.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 87593-103-50 | 8759301035087593010350 | 50 g in 1 BOX (87593-103-50)Marketed from Mar 20, 2025 |
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)
- 2% Minoxidil Serum For Women
- Generic name (nonproprietary)
- 2% minoxidil serum for women
- Active ingredients
- Minoxidil — 1 g/50g
- Dosage form
- Liquid
- Route
- Cutaneous
- Labeler
- Lance (Guangzhou) Biological Technology Co., Ltd.NDC labeler code 87593
- 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 87593-103_5d4feaaf-0587-77d5-e063-6394a90a359bSPL ID 5d4feaaf-0587-77d5-e063-6394a90a359b
- 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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.
- NDC on a medical claim
N487593010350followed by a unit qualifier and the quantityPackage 87593-0103-50. 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
The FDA listing for this product does not reference a label (SPL) set.
About NDC 87593-103
- What is NDC 87593-103?
- 87593-103 is the product NDC for 2% Minoxidil Serum For Women, Minoxidil 1 g/50g liquid, listed with the FDA by Lance (Guangzhou) Biological Technology Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- 2% Minoxidil Serum For Women.
- What is the active ingredient?
- Minoxidil.
- Who is the labeler?
- Lance (Guangzhou) Biological Technology Co., Ltd., NDC labeler code 87593. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for 2% Minoxidil Serum For Women?
- 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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| Surface x Cutie Pals Hand Sanitizer Citrus Crushalcohol | Alcohol 70 mL/100mL | LiquidTopical | I World LLC | 85179-010 |
| Minoxidil Hair Generation Serum5% minoxidil with biotin | Finasteride .1 g/100g; Minoxidil 5 g/100g | PasteTopical | Guangzhou ChuanMa International Trading Co.,Ltd. | 85593-020 |
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| everyone hand sanitizer lavender aloeethyl alcohol | Alcohol 62 mL/100mL | SprayTopical | EO Products, LLC | 54748-602 |
| Instant Hand Sanitizeralcohol | Alcohol .7 mL/mL | GelTopical | New World Imports, Inc. | 51824-020 |
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