REGOXIDINE (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
REGOXIDINE (FOR MEN)
Generic name
MINOXIDIL
Manufacturer
INNOVUS PHARMACEUTICALS, INC.
Product type
HUMAN OTC DRUG
SPL set ID
d191b3a9-0fb7-45cc-82a1-b64a79c0c125
SPL ID
7f6c711d-2ee7-46d5-8b2c-4cf643bff18e
Version
3
Effective date
2026-01-20
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:25:49
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.