Pain Relieving Cream 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
Pain Relieving Cream Analgesic
Generic name
MENTHOL, UNSPECIFIED FORM AND METHYL SALICYLATE
Manufacturer
Garcoa, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
2f736307-5cd4-4a76-9044-4aeecba096cc
SPL ID
b5e06ab5-1bf1-4605-92b2-11a8858002ff
Version
1
Effective date
2026-08-18
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:29:29
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 For external use only. ALLERGY ALERT If prone to allergic reaction from aspirin or salicylates, consult a doctor before use. When using this product •Avoid contact with eyes •Use only as directed •Perform a patch test prior to use. A transient burning sensation may occur upon application. With regular use, this sensation generally disappears after several days. •Do not apply to wounds or damaged skin •Do not bandage tightly •Do not use with a heating pad. Stop use and ask a doctor if •severe burning persists or blistering occurs •condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days. Pregnancy/Breastfeeding If pregnant or breastfeeding ask a health professional before use. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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