FDA.reportPublic FDA data

Flyleaf WART REMOVER

openFDA label record#

Cross-check layer: This is openFDA JSON-derived label data. Use the corresponding DailyMed SPL as the canonical label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Flyleaf WART REMOVER
Generic name
SALICYLIC ACID 40%
Manufacturer
Guangzhou Huixue Biotechnology Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
53f1ca40-e909-e9df-e063-6294a90a9791
SPL ID
53f1ca40-e90a-e9df-e063-6294a90a9791
Version
1
Effective date
2026-06-10
Source export date
2026-08-01
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/d245bd7ce31d1d8ed63276109973402ece6c44860774da30f25b731cd7418983/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:34:49
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. Flammable Keep away from fire and flame. Keep out of reach of children. Avoid contact with eyes, in case of contact, flush eyes with plenty of cool water. Do not swallow, if swallowed, seek medical attention or contact a Poison Control Center (1-800-222-1222) immediately.