KELAN

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: KELAN
Generic name: SILICON DIOXIDE, ARNICA MONTANA ROOT, GRAPHITE, HYPERICUM PERFORATUM, LEDUM PALUSTRE TWIG, MAGNESIUM FLUORIDE, MAGNESIUM SULFATE HEPTAHYDRATE, AND RUTA GRAVEOLENS FLOWERING TOP
Manufacturer: PEKANA Naturheilmittel GmbH
Product type: HUMAN OTC DRUG
SPL set ID: 55786d99-ee1f-490f-9023-3e6c39da86b0
SPL ID: 63d764d3-3f6c-4445-ac66-40ef9869b161
Version: 6
Effective date: 2022-12-22
Source export date: 2026-10-30
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/e37bebe0ee356110e46fe9b102632217cd5fd64caa93a64cf6ef0d92a0bfdb4c/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:51:42

Harmonized routes table
Harmonized routes
CUTANEOUS

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		KELAN	openfda.brand_name
generic name		SILICON DIOXIDE, ARNICA MONTANA ROOT, GRAPHITE, HYPERICUM PERFORATUM, LEDUM PALUSTRE TWIG, MAGNESIUM FLUORIDE, MAGNESIUM SULFATE HEPTAHYDRATE, AND RUTA GRAVEOLENS FLOWERING TOP	openfda.generic_name
manufacturer name		PEKANA Naturheilmittel GmbH	openfda.manufacturer_name
ndc	package	59469-066-30	openfda.package_ndc
ndc	package	59469-066-35	openfda.package_ndc
ndc	product	59469-066	openfda.product_ndc
ndc11	package	59469006630	derived:openfda.package_ndc
ndc11	package	59469006635	derived:openfda.package_ndc
spl id		63d764d3-3f6c-4445-ac66-40ef9869b161	id
spl set id		55786d99-ee1f-490f-9023-3e6c39da86b0	set_id
unii		877L01IZ0P	openfda.unii
unii		XK4IUX8MNB	openfda.unii
unii		5N014C7IWU	openfda.unii
unii		4QQN74LH4O	openfda.unii
unii		N94C2U587S	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		SK47B8698T	openfda.unii
unii		MUE8Y11327	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 use on open wounds! If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use. Keep out of the reach of children.

Reported adverse events (FAERS/openFDA)#

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