NDC codes

FDA NDC Directory
Product NDC (as listed)87863-021Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87863-0021Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
87863-021-0187863002101100 mg in 1 BOTTLE (87863-021-01)Marketed from Aug 1, 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)
5% Minoxidil Topical Solution
Generic name (nonproprietary)
5% minoxidil topical solution
Active ingredients
Minoxidil — 5 mg/100mg
Dosage form
Lotion/shampoo
Route
Cutaneous
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Arteriolar Vasodilation (Physiologic effect)
Identifiers
Product ID 87863-021_58e8f7a9-54a2-3db5-e063-6294a90a22e8SPL ID 58e8f7a9-54a2-3db5-e063-6294a90a22e8SPL set ID 57f7058b-68c0-66c8-e063-6394a90a5bb9UNII 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 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

N487863002101 followed by a unit qualifier and the quantity

Package 87863-0021-01. 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 on the top of the scalp.Use only on the scalp. Avoid contact with eyes. If contact occurs, rinse thoroughly with cool water.Wash hands immediately after application.This product is flammable. Keep away from fire or flame until dry.Do not use if pregnant or breastfeeding.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 87863-021

What is NDC 87863-021?
87863-021 is the product NDC for 5% Minoxidil Topical Solution, Minoxidil 5 mg/100mg lotion/shampoo, listed with the FDA by Shenzhen Jinyang E-commerce Business Department (A Sole Proprietorship). It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
5% Minoxidil Topical Solution.
What is the active ingredient?
Minoxidil.
Who is the labeler?
Shenzhen Jinyang E-commerce Business Department (A Sole Proprietorship), NDC labeler code 87863. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for 5% Minoxidil Topical Solution?
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.

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