Menthol

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: Menthol
Generic name: AMISH ORIGINS MEDICATED
Manufacturer: Amish Origins LLC
Product type: HUMAN OTC DRUG
SPL set ID: 547abe39-3af3-4d70-99dd-caf8d67feda2
SPL ID: 28656961-9c32-9983-e063-6394a90ae6e4
Version: 26
Effective date: 2024-12-03
Source export date: 2026-10-30
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/a900515c00f4d0d29f88cc94ee68daf127f036296f87a6b4a8a3f964cd0433c0/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:49:03

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Menthol	openfda.brand_name
generic name		AMISH ORIGINS MEDICATED	openfda.generic_name
manufacturer name		Amish Origins LLC	openfda.manufacturer_name
ndc	package	62212-252-02	openfda.package_ndc
ndc	package	62212-252-01	openfda.package_ndc
ndc	package	62212-252-04	openfda.package_ndc
ndc	package	62212-252-03	openfda.package_ndc
ndc	product	62212-252	openfda.product_ndc
ndc11	package	62212025203	derived:openfda.package_ndc
ndc11	package	62212025202	derived:openfda.package_ndc
ndc11	package	62212025204	derived:openfda.package_ndc
ndc11	package	62212025201	derived:openfda.package_ndc
rxcui		727161	openfda.rxcui
spl id		28656961-9c32-9983-e063-6394a90ae6e4	id
spl set id		547abe39-3af3-4d70-99dd-caf8d67feda2	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, As Directed! Avoid contact with eyes or other sensitive areas. If prone to allergic reaction from asprin or salicylate, consult your doctor before using. If conditions persist pore than seven days, consult your doctor If pregnant or breast-feeding, ask a health professional before use. Do not bandange tightly or use a heating pad May irritate sensitive skin Keep ointment out of reach of children

Reported adverse events (FAERS/openFDA)#

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