Eagle Brand Medicated Oil

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
Generic name: MENTHOL, METHYL SALICYLATE
Manufacturer: PT. EAGLE INDO PHARMA
Product type: HUMAN OTC DRUG
SPL set ID: 5071f145-49f7-0855-e063-6394a90a8f26
SPL ID: 5071f145-49f8-0855-e063-6394a90a8f26
Version: 1
Effective date: 2026-04-27
Source export date: 2026-10-12
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:46:34

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	openfda.brand_name
generic name		MENTHOL, METHYL SALICYLATE	openfda.generic_name
manufacturer name		PT. EAGLE INDO PHARMA	openfda.manufacturer_name
ndc	package	60954-018-36	openfda.package_ndc
ndc	package	60954-018-24	openfda.package_ndc
ndc	product	60954-018	openfda.product_ndc
ndc11	package	60954001836	derived:openfda.package_ndc
ndc11	package	60954001824	derived:openfda.package_ndc
rxcui		1293435	openfda.rxcui
rxcui		1293430	openfda.rxcui
spl id		5071f145-49f8-0855-e063-6394a90a8f26	id
spl set id		5071f145-49f7-0855-e063-6394a90a8f26	set_id
unii		L7T10EIP3A	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 use only as directed. do not get into eyes or mucous membranes. do not apply to wounds or damaged skin. do not bandage tightly. Stop use and ask doctor if excessive skin irritation develops. pain worsens or does not improve within 7 days, or clears up and appears again in a few days. Keep this drug 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.