DG Health Cold n Hot Pain Relieving Topical Analgesic

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
DG Health Cold n Hot Pain Relieving Topical Analgesic
Generic name
MENTHOL, UNSPECIFIED FORM
Manufacturer
Dolgencorp Inc
Product type
HUMAN OTC DRUG
SPL set ID
8fe13b85-ab74-42f8-a664-d3d2959921ac
SPL ID
c4b075fb-db59-4239-aede-60854bc6d1f8
Version
4
Effective date
2024-10-30
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:26:27
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Test on a small patch of skin before applying generously. When using this product use only as directed avoid contact with the eyes and mucous membranes do not apply to wounds or damaged skin do not bandage tightly do not use with heating pads or other heating devices if redness is present, discontinue use and consult a doctor if skin irritation occurs, discontinue use a transient burning sensation may occur upon application but generally disappears in several days Stop use and consult a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Flammable keep away from fire or flame If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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