Lakeim FUNGAL NAIL RENEWAL Kit

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
Lakeim FUNGAL NAIL RENEWAL Kit
Generic name
FUNGAL NAIL RENEWAL KIT
Manufacturer
Guangzhou Jingliang Cosmetics Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
4b6aae50-b219-beee-e063-6394a90ab415
SPL ID
4b6aae62-86ad-c1c5-e063-6394a90acefe
Version
1
Effective date
2026-02-22
Source export date
2026-11-06
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:45:28
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external application solely on fungal-affected nails; refrain from using on healthy nails. Avoid applying to damaged skin to prevent potential discomfort or pain. Store out of reach of children. Do not ingest and avoid contact with eyes. In case of eye exposure, rinse thoroughly with water for 15 minutes. If ingested, seek immediate medical assistance or contact a Poison Control Center without delay.

Reported adverse events (FAERS/openFDA)#

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