SUPREN

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: SUPREN
Generic name: ARSENIC TRIOXIDE, SULFURIC ACID, CHAMAELIRIUM LUTEUM ROOT, GOLDENSEAL, WOOD CREOSOTE, LEMNA MINOR, MAGNESIUM FLUORIDE, AND SILICON DIOXIDE
Manufacturer: PEKANA Naturheilmittel GmbH
Product type: HUMAN OTC DRUG
SPL set ID: 3b34740c-b181-4f05-9858-15b7211a4c67
SPL ID: 5882f99c-53c3-428c-9991-2e409eaaf9d4
Version: 5
Effective date: 2022-12-22
Source export date: 2026-10-12
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:59:51

Harmonized routes table
Harmonized routes
ORAL

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		SUPREN	openfda.brand_name
generic name		ARSENIC TRIOXIDE, SULFURIC ACID, CHAMAELIRIUM LUTEUM ROOT, GOLDENSEAL, WOOD CREOSOTE, LEMNA MINOR, MAGNESIUM FLUORIDE, AND SILICON DIOXIDE	openfda.generic_name
manufacturer name		PEKANA Naturheilmittel GmbH	openfda.manufacturer_name
ndc	package	59469-060-10	openfda.package_ndc
ndc	product	59469-060	openfda.product_ndc
ndc11	package	59469006010	derived:openfda.package_ndc
spl id		5882f99c-53c3-428c-9991-2e409eaaf9d4	id
spl set id		3b34740c-b181-4f05-9858-15b7211a4c67	set_id
unii		5N014C7IWU	openfda.unii
unii		621HHM46SV	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		O40UQP6WCF	openfda.unii
unii		ZW3Z11D0JV	openfda.unii
unii		3JYG22FD73	openfda.unii
unii		DQV54Y5H3U	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

Warning 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. Protect from light and heat. Tamper Evident Do not use this product if tamper evident strip is broken or removed from base of cap.

Reported adverse events (FAERS/openFDA)#

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