BonicaEaseX Menthol Pain Relieving

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
BonicaEaseX Menthol Pain Relieving
Generic name
MENTHOL, UNSPECIFIED FORM
Manufacturer
Planet (Anhui) Pharmaceutical Co.,Ltd
Product type
HUMAN OTC DRUG
SPL set ID
4d84b4fb-8f55-4b2b-b261-858edb7f3144
SPL ID
4f1bd117-096a-4915-e063-6394a90a8a43
Version
1
Effective date
2026-04-10
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:55:26
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 • Please read all directions and warnings as follows and use only as directed. For external use only. • Flammable: Keep away from excessive heat or open flame. Do not heat, microwave, add to hot water or any container where heating water may cause splattering and result in burns. • If pregnant or breast-feeding, ask a health professional before use. • Do not bandage tightly. • Avoid contact with the eyes. • Do not apply to wounds or damaged skin Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center right away. Do not use • Alone if you are under the age of 12, please consult a doctor. • If you’re allergic to the listed ingredients. • If the package arrives damaged or opened. • at the same time as other topical analgesics. • on mucous membranes, cuts, broken, swollen, or irritated skin. Stop use and ask a doctor if • if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. • if you experience any signs of deterioration or skin injury, such as redness, irritation, swelling, or blistering. • if the arthritic pain persists for more than 10 days, or redness is presen

Reported adverse events (FAERS/openFDA)#

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