Eagle Brand Medicated Plaster Extra Strength

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
Eagle Brand Medicated Plaster Extra Strength
Generic name
MENTHOL, CAPSAICIN
Manufacturer
Borden Company (Private) Limited
Product type
HUMAN OTC DRUG
SPL set ID
2f2a4080-d538-1c6a-e063-6394a90ae51c
SPL ID
30083d52-4a37-eabf-e063-6294a90ac95f
Version
2
Effective date
2025-03-10
Source export date
2026-10-27
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/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 19:49:22
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 When using this product ▪ Avoid contact with eyes or on mucous membranes. ▪ Do not apply to wounds or damaged skin. ▪ Do not bandage tightly. ▪ Do not apply wiht external heat, such as heating pad. ▪ Do not use otherwise than as directed Stop use and ask doctor if ▪ Condition worsens. ▪ Symptoms persist for more than 7 days. ▪ Clear up and occur again within a few days, discontinue use of this product and consult a doctor. ▪ Skin reactions such as redness, itching, rash, excessive irritation, burning sensation, swelling or blistering occurs. If pregnant or breast-feeding Ask a health professional before use. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Centre right away.

Reported adverse events (FAERS/openFDA)#

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