Magsoothium CBD Body Lavender

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: Magsoothium CBD Body Lavender
Generic name: MENTHOL
Manufacturer: Ubu/Elements, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: f9b87fbe-b889-67a1-e053-6394a90acbcd
SPL ID: 4615f244-fb02-fa47-e063-6294a90aba6e
Version: 3
Effective date: 2025-12-16
Source export date: 2026-10-27
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/eeb012fd0992efa4f76b2aef09dd5f84150b96392c46717c44deabcc4e3581c1/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:41:25

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Magsoothium CBD Body Lavender	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Ubu/Elements, Inc.	openfda.manufacturer_name
ndc	package	83262-003-01	openfda.package_ndc
ndc	product	83262-003	openfda.product_ndc
ndc11	package	83262000301	derived:openfda.package_ndc
spl id		4615f244-fb02-fa47-e063-6294a90aba6e	id
spl set id		f9b87fbe-b889-67a1-e053-6394a90acbcd	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. when using this product Use only as directed Do not bandage or cover the area being treated Do not apply ice or heating pad in conjunction with this product Do not use with any medical device or other device Do not combine with any other toipcal treatment Avoid contact with eyes or mucous membrane Do not apply to wounds or damaged skin 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.