Eagle Brand Medicated Oil Refresh

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 Refresh
Generic name: CAMPHOR, MENTHOL
Manufacturer: Borden Company (Private) Limited
Product type: HUMAN OTC DRUG
SPL set ID: 09243a23-1f17-f77b-e063-6394a90a0b22
SPL ID: 20145641-991d-d184-e063-6394a90a4af5
Version: 4
Effective date: 2024-08-19
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 05:20:03

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Eagle Brand Medicated Oil Refresh	openfda.brand_name
generic name		CAMPHOR, MENTHOL	openfda.generic_name
manufacturer name		Borden Company (Private) Limited	openfda.manufacturer_name
ndc	package	43405-013-36	openfda.package_ndc
ndc	package	43405-013-24	openfda.package_ndc
ndc	product	43405-013	openfda.product_ndc
ndc11	package	43405001324	derived:openfda.package_ndc
ndc11	package	43405001336	derived:openfda.package_ndc
rxcui		2672336	openfda.rxcui
spl id		20145641-991d-d184-e063-6394a90a4af5	id
spl set id		09243a23-1f17-f77b-e063-6394a90a0b22	set_id
unii		L7T10EIP3A	openfda.unii
unii		5TJD82A1ET	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 a 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 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.