MEOLY Fungal Nail Renewal

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
MEOLY Fungal Nail Renewal
Generic name
FUNGAL NAIL RENEWAL
Manufacturer
Shenzhen Xinxin Yunhai Technology Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
487d2e22-6328-893f-e063-6394a90a9dff
SPL ID
487d2e22-6329-893f-e063-6394a90a9dff
Version
1
Effective date
2026-01-16
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 05:35:11
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 • Do not use on children under 2 years of age unless directed by a doctor ■ Avoid contact with eyes. If contact occurs, rinse thoroughly with water Purpose ....Antifungal ▪ Stop use and ask a doctor if irritation, redness, or symptoms worsen or persist ■ Keep out of reach of children ■ If swallowed, rinse mouth and seek medical attention or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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