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
2026-11-06
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/2026-11-06/2cac198adf50bf0f7077ca012f418bbee1fb171f907f83d6a83048d9770d345b/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 08:11:45
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 • 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.