HealthWise Soothing Cold Therapy 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
HealthWise Soothing Cold Therapy Gel
Generic name
MENTHOL 4%
Manufacturer
Veridian Healthcare
Product type
HUMAN OTC DRUG
SPL set ID
1f09ccdd-09d8-6a8d-e063-6394a90a184f
SPL ID
1f2ef992-1262-4b39-e063-6394a90a6dd9
Version
2
Effective date
2024-08-08
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:16:01
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 Flammable: keep away from excessive heat or open flame Ask a doctor before use if you have sensitive skin When using this product, do not When using this product: ■ avoid contact with eyes or mucous membranes ■ do not apply to wounds or damaged skin ■ do not use with other ointments, creams, sprays or liniments ■do not apply to irritated skin or if excessive irritation develops ■do not bandage ■ wash hands after use with cool water ■do not use with a heating pad or device Stop use and ask a doctor if Stop use and ask a doctor if: the condition worsens, if the symptoms last more than 7 days or clear up and reoccur If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center (800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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