Dr. Carrasco 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
Dr. Carrasco Pain Relief
Generic name
MENTHOL
Manufacturer
Carrasco Enterprises, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
befa8526-f468-428e-a829-422c2ea48612
SPL ID
4ff6ae0f-1090-c66a-e063-6294a90a26a0
Version
6
Effective date
2026-04-21
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:20:14
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. Not intended for ingestion. Do not use: On damaged or broken skin. When using this product Avoid contact with the eyes. • Do not bandage tightly. Stop use and ask a doctor if: Rash or irritation develops and lasts. • condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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