Arctic Ice Pain Relieving Gel

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
Arctic Ice Pain Relieving Gel
Generic name
MENTHOL
Manufacturer
ONEST LIMITED
Product type
HUMAN OTC DRUG
SPL set ID
c63ef7a5-d649-4fba-9361-d37f1150e21d
SPL ID
58c4e4f3-b9ec-ed2a-e063-6394a90af35a
Version
1
Effective date
2026-08-11
Source export date
2026-09-28
Source partition
14
Source file
https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:41:32
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. Avoid contact with eyes. Ask a doctor before use if you have a cough associated with: Smoking Excessive phlegm Asthma Emphysema Persistent or chronic cough When using this product, do not: Heat, microwave, or add to hot water or any container where heating water may cause splattering and result in burns Use in eyes or directly on mucous membranes Take by mouth or place in nostrils Apply to wounds or damaged skin Bandage skin Consult a doctor and discontinue Use: If condition worsens, persists more than 1 week or tends to recur. Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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