FluMisch Minoxidil Foam

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
FluMisch Minoxidil Foam
Generic name
MINOXIDIL,BIOTIN
Manufacturer
Beijing JUNGE Technology Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
2d34dc32-47d8-590d-e063-6294a90a2f2d
SPL ID
2d34dc32-47d9-590d-e063-6294a90a2f2d
Version
1
Effective date
2025-02-02
Source export date
2026-09-28
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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:47:55
Harmonized routes table
Harmonized routes
EXTRACORPOREAL

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

For external use only. Extremely Flammable: Avoid fire, flame, or smoking during andimmediately following application.

Reported adverse events (FAERS/openFDA)#

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