Easment DMSO cream

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: Easment DMSO cream
Generic name: MENTHOL 1.00%
Manufacturer: Easment LLC
Product type: HUMAN OTC DRUG
SPL set ID: 48f5544e-1cfd-864a-e063-6394a90a71f1
SPL ID: 48f5544e-1cfe-864a-e063-6394a90a71f1
Version: 1
Effective date: 2026-01-22
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 05:19:04

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		Easment DMSO cream	openfda.brand_name
generic name		MENTHOL 1.00%	openfda.generic_name
manufacturer name		Easment LLC	openfda.manufacturer_name
ndc	package	87352-002-01	openfda.package_ndc
ndc	product	87352-002	openfda.product_ndc
ndc11	package	87352000201	derived:openfda.package_ndc
rxcui		2475473	openfda.rxcui
spl id		48f5544e-1cfe-864a-e063-6394a90a71f1	id
spl set id		48f5544e-1cfd-864a-e063-6394a90a71f1	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

For external use only. on wounds or damaged skin with a heating pad if allergic to ingredient in the product Avoidcontact with the eyes Do not bandage tightly rash or irritation developsand lasts condition worsens, or if symptoms persist for more than 7 days or clear up ad occur again within a few days If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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