Eagle Brand Medicated Oil Aromatic

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 Oil Aromatic
Generic name: CAMPHOR, MENTHOL, METHYL SALICYLATE
Manufacturer: Borden Company (Private) Limited
Product type: HUMAN OTC DRUG
SPL set ID: 0e808f89-62dc-3790-e063-6394a90a2351
SPL ID: 1861aad8-8456-0dbc-e063-6394a90ad5d3
Version: 2
Effective date: 2024-05-13
Source export date: 2026-10-12
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:28:35

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Eagle Brand Medicated Oil Aromatic	openfda.brand_name
generic name		CAMPHOR, MENTHOL, METHYL SALICYLATE	openfda.generic_name
manufacturer name		Borden Company (Private) Limited	openfda.manufacturer_name
ndc	package	43405-014-36	openfda.package_ndc
ndc	package	43405-014-24	openfda.package_ndc
ndc	product	43405-014	openfda.product_ndc
ndc11	package	43405001436	derived:openfda.package_ndc
ndc11	package	43405001424	derived:openfda.package_ndc
rxcui		1654728	openfda.rxcui
spl id		1861aad8-8456-0dbc-e063-6394a90ad5d3	id
spl set id		0e808f89-62dc-3790-e063-6394a90a2351	set_id
unii		L7T10EIP3A	openfda.unii
unii		5TJD82A1ET	openfda.unii
unii		LAV5U5022Y	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 getting into the eyes or on mucous membranes. Do not apply to wounds or damaged skin. Do not bandage tightly. Do not use otherwise than as directed. Stop use and ask doctor if Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor. If pregnant or breast-feeding Ask a health professional before use. Keep ouf 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.