Home NDC 87022-006 hair growth solution
Product NDC 87022-006
11-digit product format 870220006
Labeler code 87022
Product ID 87022-006_3d84e916-85db-c89f-e063-6394a90a66e7
Type HUMAN OTC DRUG
Nonproprietary name MINOXIDIL
Dosage form LIQUID
Route TOPICAL
Labeler LABORATORIO MK SRL
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-13
Marketing end 2027-08-12
Substance MINOXIDIL
Active strength 5 mg/20mL
Pharmacologic classes Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
NDC exclude flag No
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 87022-006 87022-006-22 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 87022-006 87022-006-21 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
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 hair growth solution Active Ingredients# Ingredient, Strength table Ingredient Strength MINOXIDIL 5 mg/20mL
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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87022-006-21 hair growth solution 20 mL in 1 BOTTLE LIQUID 20 3 87022-006-22 hair growth solution 120 mL in 1 BOX LIQUID 120 3
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 87022-006-21 87022000621 20 mL in 1 BOTTLE (87022-006-21) 20 ml 2025-08-13 2027-08-12 Yes No Historical 87022-006-22 87022000622 120 mL in 1 BOX (87022-006-22) 120 ml 2025-08-13 2027-08-12 No No Historical