EITIKO Minoxidil Hair Regrowth Treatment

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
EITIKO Minoxidil Hair Regrowth Treatment
Generic name
MINOXIDIL
Manufacturer
Guangzhou Ariel Medical Technology Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
5aa2a552-f8b5-f11a-e063-6394a90abb1a
SPL ID
5aa2a565-bb5f-63ea-e063-6294a90aa972
Version
1
Effective date
2026-09-04
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:37:59
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

For external use only. Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Keep out of reach of children. Discontinue use if any irritation or adverse reaction occurs. If you are pregnant, nursing, or have any underlying medical conditions, consult your healthcare provider before using the product.

Reported adverse events (FAERS/openFDA)#

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