Mentholatum Original

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: Mentholatum Original
Generic name: CAMPHOR, MENTHOL
Manufacturer: The Mentholatum Company
Product type: HUMAN OTC DRUG
SPL set ID: 19e4b812-67c6-49fd-833a-b432100363f5
SPL ID: 292b4ddf-f5d8-d052-e063-6394a90a5f1d
Version: 6
Effective date: 2024-12-13
Source export date: 2026-10-12
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:41:18

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Mentholatum Original	openfda.brand_name
generic name		CAMPHOR, MENTHOL	openfda.generic_name
manufacturer name		The Mentholatum Company	openfda.manufacturer_name
ndc	package	10742-0002-2	openfda.package_ndc
ndc	package	10742-0002-4	openfda.package_ndc
ndc	package	10742-0002-3	openfda.package_ndc
ndc	package	10742-0002-1	openfda.package_ndc
ndc	product	10742-0002	openfda.product_ndc
ndc11	package	10742000204	derived:openfda.package_ndc
ndc11	package	10742000203	derived:openfda.package_ndc
ndc11	package	10742000201	derived:openfda.package_ndc
ndc11	package	10742000202	derived:openfda.package_ndc
rxcui		1042667	openfda.rxcui
rxcui		1042663	openfda.rxcui
spl id		292b4ddf-f5d8-d052-e063-6394a90a5f1d	id
spl set id		19e4b812-67c6-49fd-833a-b432100363f5	set_id
unii		L7T10EIP3A	openfda.unii
unii		N20HL7Q941	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 do not get into eyes do not apply to wounds or to damaged skin do not bandage tightly do not heat, microwave, or add to hot water as this may cause splattering and result in burns Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days 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.