Cetilar

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: Cetilar
Generic name: MENTHOL 1.4%
Manufacturer: PharmaNutra Usa Corp.
Product type: HUMAN OTC DRUG
SPL set ID: 2dd14bd4-b4e1-bc7d-e063-6394a90a1e59
SPL ID: 2dd14e68-9b33-bad8-e063-6394a90a9fc1
Version: 1
Effective date: 2025-02-04
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:24:54

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Cetilar	openfda.brand_name
generic name		MENTHOL 1.4%	openfda.generic_name
manufacturer name		PharmaNutra Usa Corp.	openfda.manufacturer_name
ndc	package	84797-000-49	openfda.package_ndc
ndc	product	84797-000	openfda.product_ndc
ndc11	package	84797000049	derived:openfda.package_ndc
rxcui		2391332	openfda.rxcui
spl id		2dd14e68-9b33-bad8-e063-6394a90a9fc1	id
spl set id		2dd14bd4-b4e1-bc7d-e063-6394a90a1e59	set_id
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. Avoid contact with eyes When using this product Do not bandage tightly do not apply to wounds or damage skin Stop use and ask a doctor if condition worsens if symptoms persist for more than 7 days or clear up and occur again within a few days 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 Center right away

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.