HEMPCIN Advanced Topical Pain Relief Cream

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
HEMPCIN Advanced Topical Pain Relief Cream
Generic name
MENTHOL
Manufacturer
Pedicis Research, LLC
Product type
HUMAN OTC DRUG
SPL set ID
97f5e300-b780-4694-a681-60d5e0cfad65
SPL ID
0973b73d-5dd0-0986-e063-6294a90a5917
Version
2
Effective date
2023-11-05
Source export date
2026-10-12
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/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:51:34
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 • Avoid contact with the eyes • Do not apply to wounds or damaged skin • Do not bandage tightly • Cap tube tightly and store at room temperature away from heat When using this product: • do not use in large quantities particularly over raw surfaces or blistered areas • do not exceed recommended doses unless recommended by a doctor Stop use and ask a doctor if: • allergic reaction occurs • condition worsens or does not improve within 7 days • symptoms clear up and do not return within a few days • you notice any unusual effects Keep out of the reach of children: If swallowed get medical help or call a Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

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