Eagle Brand Medicated Roll On 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 Roll On Refresh
Generic name: CAMPHOR, MENTHOL
Manufacturer: PT. EAGLE INDO PHARMA
Product type: HUMAN OTC DRUG
SPL set ID: 09235f26-2262-6ca2-e063-6394a90ad8f1
SPL ID: 507b9495-e9a3-7fba-e063-6394a90a8d84
Version: 2
Effective date: 2026-04-27
Source export date: 2026-10-27
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/2026-10-27/55ffdfed5c29f1b4aed512886bd3fb7831e157cc4948137779971a558752ed2b/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:06:51

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		M017	openfda.application_number
brand name		Eagle Brand Medicated Roll On Refresh	openfda.brand_name
generic name		CAMPHOR, MENTHOL	openfda.generic_name
manufacturer name		PT. EAGLE INDO PHARMA	openfda.manufacturer_name
ndc	package	60954-012-08	openfda.package_ndc
ndc	product	60954-012	openfda.product_ndc
ndc11	package	60954001208	derived:openfda.package_ndc
rxcui		2672336	openfda.rxcui
spl id		507b9495-e9a3-7fba-e063-6394a90a8d84	id
spl set id		09235f26-2262-6ca2-e063-6394a90ad8f1	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.