FDA label f5c9e0e2-8304-123b-e053-2995a90a0f60

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)

SPL set ID
0186162c-da24-43da-8a37-4d57561955b2
SPL ID
f5c9e0e2-8304-123b-e053-2995a90a0f60
Version
1
Effective date
2023-02-28
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:30:42

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

Warning For external use only. Avoid eye contact. This product is not for women.Finasteride has been shown to cause birth defects in women who are pregnant or may become pregnant. Be sure this product is never handled or used by women. Keep out of reach of children. Minoxidil has been shown to increase unwanted body hair. Use as directed.

Reported adverse events (FAERS/openFDA)#

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