Doctor Hoys Pain Relief 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
Doctor Hoys Pain Relief Gel
Generic name
MENTHOL, CAMPHOR (SYNTHETIC)
Manufacturer
Dynamic Blending Specialists, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
50123bb9-d5d8-4ba6-ab94-8ed95fe0f5a8
SPL ID
4769df6d-225f-5a0d-e063-6394a90af652
Version
4
Effective date
2026-01-02
Source export date
2026-09-28
Source partition
14
Source file
https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:41:02
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 • Use as directed • Avoid contact with eyes or mucus membranes • Do not apply to open wounds, irritated or damaged skin Keep Out of reach of children If swallowed, get medical help or contact a Poison Control Center immediately If pregnant or breast feeding, • ask a health professional before use • Discontinue use of this product and consult a physician if condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days • Use caution with wrap or heating pad.

Reported adverse events (FAERS/openFDA)#

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