Quality Choice 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
Quality Choice Cold Therapy Gel
Generic name
MENTHOL
Manufacturer
Chain Drug Marketing Association, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
f9c659cd-e7fa-ac2d-e053-6294a90a2573
SPL ID
4721fb64-bc29-b450-e063-6294a90a056e
Version
4
Effective date
2025-12-29
Source export date
2026-11-06
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:45:12
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: ■ 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 an ask a doctor if condition worsens, if symptoms last more than 7 days or clear up and reoccur If pregnant or breastfeeding: ask a health professional before use Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away

Reported adverse events (FAERS/openFDA)#

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