Meijer Cold Therapy 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
Meijer Cold Therapy Pain Relieving
Generic name
MENTHOL
Manufacturer
Meijer Inc
Product type
HUMAN OTC DRUG
SPL set ID
1c5b55e3-f859-71b6-e063-6294a90a633b
SPL ID
1f2c33f6-a86b-a504-e063-6394a90a6fb4
Version
2
Effective date
2024-08-08
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:44:31
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 When using this product When using this product ■ Use only as directed ■Rare cases of serious burns have been reported with products of this type ■Don't bandage tightly or use with heating pad ■Avoid contact with eyes and mucous membranes ■Don't apply to wounds or damaged skin ■Do not use at the same time as other topical analgesics. Stop use and Consult a doctor if Stop use and consult a doctor if ■ Condition worsens ■ Redness is present ■ Irritation develops ■ Symptoms persist for more than 7 days or clear up and occur again within a few days ■ You experience signs of skin injury, such as pain, swelling, or blistering where the product was applied. If pregnant or breastfeeding ask a health professional before use Keep out of reach of children Keep out of reach of children. Do not use on infants. 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.