Dollar General Cold Therapy Pain Relief

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
Dollar General Cold Therapy Pain Relief
Generic name
MENTHOL 5%
Manufacturer
Dolgencorp, LLC
Product type
HUMAN OTC DRUG
SPL set ID
ff3284d1-e73c-93bf-e053-6294a90aaf4e
SPL ID
29a5a74a-6741-39aa-e063-6294a90a5ddd
Version
5
Effective date
2024-12-19
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:24:47
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 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: ■ 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 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.