5% Minoxidil Topical Solution

Product NDC: 87863-021
Requested package NDC: 87863-021-01
11-digit product format: 878630021
Labeler code: 87863
Product ID: 87863-021_58e8f7a9-54a2-3db5-e063-6294a90a22e8
Type: HUMAN OTC DRUG
Nonproprietary name: 5% Minoxidil Topical Solution
Dosage form: LOTION/SHAMPOO
Route: CUTANEOUS
Labeler: Shenzhen Jinyang E-commerce Business Department (A Sole Proprietorship)
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2026-08-01
Substance: MINOXIDIL
Active strength: 5 mg/100mg
Pharmacologic classes: Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: 5% Minoxidil Topical Solution
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MINOXIDIL	5 mg/100mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5965120SH1	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
57f7058b-68c0-66c8-e063-6394a90a5bb9	Available on FDA.report

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
5% Minoxidil Topical Solution	5% MINOXIDIL TOPICAL SOLUTION	Shenzhen Jinyang E-commerce Business Department (A Sole Proprietorship)	57f7058b-68c0-66c8-e063-6394a90a5bb9	2026-08-13	Warnings	Exact identifier ndc (package): 87863-021-01 ndc (product): 87863-021 ndc11 (package): 87863002101

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5965120SH1	MINOXIDIL	38304-91-5	MINOXIDIL

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
87863-021-01	87863002101	100 mg in 1 BOTTLE (87863-021-01)	100 mg	2026-08-01	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
5% Minoxidil Topical Solution	Shenzhen Jinyang E-commerce Business Department (A Sole Proprietorship)	2026-08-13	HUMAN OTC DRUG LABEL	3