Relief Flex

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
Relief Flex
Generic name
MENTHOL
Manufacturer
Beone Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
49e6f0ef-78fb-26fe-e063-6294a90a6655
SPL ID
49e6f0ef-78fc-26fe-e063-6294a90a6655
Version
1
Effective date
2026-02-03
Source export date
2026-10-27
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/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:59:02
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 wounds or damaged skin with a heating pad if you are allergic to menthol or any of the ingredients in this product ■ When using this product avoid contact with eyes or mucous membranes do not bandage tightly use only as directed keep away from excessive heat ■ Stop use and ask a doctor if rash occurs ■ Keep out of reach of children , If product is 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.