Nizoral Hair Regrowth Treatment for Men

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Nizoral Hair Regrowth Treatment for Men
Generic name
MINOXIDIL
Manufacturer
Kramer Laboratories
Product type
HUMAN OTC DRUG
SPL set ID
d3260777-d56a-4a35-ac82-b0e8e8021517
SPL ID
2052b831-955b-483d-8e63-1d01483c8313
Version
1
Effective date
2026-03-04
Source export date
2026-10-23
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-23/e2a780351c9d52ec13a8c93757e95e68824c68ebed04761d4eea108c6b76cf54/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
003b0607e7bf4d3ce17ccc0942e221303b4f62b17a6a00c54547eda454293380
Import run
20261026T035824Z
Imported at
2026-10-26 04:30:44
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. For use by men only. Extremely Flammable: Avoid fire, flame, or smoking during and immediately following application.

Reported adverse events (FAERS/openFDA)#

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