Icy Hot Medicated

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
Icy Hot Medicated
Generic name
MENTHOL
Manufacturer
Lead Chemical Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
d4e13689-8973-4041-9f33-e710547dcdee
SPL ID
62c6f235-4861-4faf-8273-dbd8a8b23ecc
Version
13
Effective date
2025-04-21
Source export date
2026-11-06
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/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 08:01:14
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 Icy Hot Arm, Neck and Leg Patches; and Icy Hot XL Patches • use only as directed. Read and follow all directions and warnings on this label. • avoid contact with eyes and mucous membranes • rare cases of serious burns have been reported with products of this type • do not apply to wounds or damaged, broken or irritated skin • do not bandage tightly or apply local heat (such as heating pads) to the area of use • a transient burning sensation may occur upon application but generally disappears in several days Stop use and ask a doctor if Icy Hot Arm, Neck and Leg Patches; and Icy Hot XL Patches • condition worsens • redness is present • irritation develops • symptoms persist for more than 7 days or clear up and occur again within a few days • you experience signs of skin injury, such as pain, swelling, or blistering where the product was 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.