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: 2026-09-28
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 05:18:21

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Eagle Brand Medicated Plaster Extra Strength	openfda.brand_name
generic name		MENTHOL, CAPSAICIN	openfda.generic_name
manufacturer name		Borden Company (Private) Limited	openfda.manufacturer_name
ndc	package	43405-301-05	openfda.package_ndc
ndc	product	43405-301	openfda.product_ndc
ndc11	package	43405030105	derived:openfda.package_ndc
rxcui		853136	openfda.rxcui
spl id		30083d52-4a37-eabf-e063-6294a90ac95f	id
spl set id		2f2a4080-d538-1c6a-e063-6394a90ae51c	set_id
unii		S07O44R1ZM	openfda.unii
unii		L7T10EIP3A	openfda.unii

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.