2.5% Menthol PAIN RELIEF

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
2.5% Menthol PAIN RELIEF
Generic name
MENTHOL
Manufacturer
Nantong Health & Beyond Hygienic Products Inc.
Product type
HUMAN OTC DRUG
SPL set ID
8075ba60-772c-4d1a-8584-722bb3e539be
SPL ID
4a21330e-6d27-2425-e063-6294a90a021d
Version
1
Effective date
2026-02-05
Source export date
2026-09-28
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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:29:19
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 • on a child under 12 years of age with arthritis-like conditions Ask a doctor before use if you have redness over the affected area. When using this product • avoid contact with eyes or mucous membranes • do not bandage tightly Stop use and ask a doctor if • condition worsens or symptoms persist for more than 7 days • symptoms clear up and occur again within a few days • excessive skin irritation occurs Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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