Cycle

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
Cycle
Generic name
MENTHOL
Manufacturer
La Mend, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
cfc0bcde-ef91-1e6c-e053-2a95a90ab79e
SPL ID
0bf1202d-1d5a-7707-e063-6394a90a8ce4
Version
3
Effective date
2023-12-07
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:40:23
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 use only as directed do not use with other topical products do not use on open wounds, damaged or irritated skin do not bandage tightly or apply local heat to this area, like heating pads in rare cases, burns have been reported for products of this type, containing menthol Stop use and ask a doctor if confiditon worsens redness or irritation develop symptoms last more than 7 days or clear up and occur again within a few days you experience burning, swelling, or blistering where applied If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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