KT HELATH SOOTHE MAGNESIUM, 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: KT HELATH SOOTHE MAGNESIUM, LAVENDER
Generic name: ARNICA MONTANA WHOLE
Manufacturer: KT Health LLC
Product type: HUMAN OTC DRUG
SPL set ID: 1d993fe0-2c46-426c-8922-388723e744f4
SPL ID: 2dcb305a-74cc-95cb-e063-6394a90a13a4
Version: 1
Effective date: 2025-02-10
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:53:58

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 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		KT HELATH SOOTHE MAGNESIUM, LAVENDER	openfda.brand_name
generic name		ARNICA MONTANA WHOLE	openfda.generic_name
manufacturer name		KT Health LLC	openfda.manufacturer_name
ndc	package	73044-106-01	openfda.package_ndc
ndc	product	73044-106	openfda.product_ndc
ndc11	package	73044010601	derived:openfda.package_ndc
spl id		2dcb305a-74cc-95cb-e063-6394a90a13a4	id
spl set id		1d993fe0-2c46-426c-8922-388723e744f4	set_id
unii		O80TY208ZW	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 Do not apply to wounds or damaged skin. Do not bandage tightly. Avoid contact with eyes. If conditions worsen or persist for more than 7 days, discontinue use of this product and consult a physician. Ask a doctor before use: If pregnant or breast feeding Children under 2 years of age Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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