FDA.reportPublic FDA data

LK Herbal Patch

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
LK Herbal Patch
Generic name
L-MENTHOL
Manufacturer
CAI Industries Corp.
Product type
HUMAN OTC DRUG
SPL set ID
c56241b3-ef7a-40ee-a89a-754a580b0118
SPL ID
3ce1efcd-fab6-783f-e063-6294a90aecdf
Version
1
Effective date
2025-08-21
Source export date
2026-08-01
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/286b06ef66f7efdb8cdf48688678b429950d1b94558fe44fcd6cc6eb20c2100b/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:04:12
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 When using this product avoid contact with the eyes or mucous membranes do not use on wounds or broken skin Stop use and ask a doctor if conditions worsen excessive skin irritation develops nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash occurs symptoms persists for more than 7 days If pregnant or breast-feeding , ask a doctor before use. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away.