PROALLER

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: PROALLER
Generic name: AILANTHUS ALTISSIMA WHOLE, OKOUBAKA AUBREVILLEI BARK, EUPHRASIA STRICTA, GRATIOLA OFFICINALIS, JUGLANS REGIA WHOLE, SMILAX REGELII ROOT, AND TARAXACUM OFFICINALE WHOLE
Manufacturer: PEKANA Naturheilmittel
Product type: HUMAN OTC DRUG
SPL set ID: 101ff372-e618-4c06-bad1-e2bfbc9e4349
SPL ID: 78ed18a7-da36-4ead-be28-92693f46c272
Version: 5
Effective date: 2022-12-19
Source export date: 2026-10-12
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:28:13

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		PROALLER	openfda.brand_name
generic name		AILANTHUS ALTISSIMA WHOLE, OKOUBAKA AUBREVILLEI BARK, EUPHRASIA STRICTA, GRATIOLA OFFICINALIS, JUGLANS REGIA WHOLE, SMILAX REGELII ROOT, AND TARAXACUM OFFICINALE WHOLE	openfda.generic_name
manufacturer name		PEKANA Naturheilmittel	openfda.manufacturer_name
ndc	package	59469-116-10	openfda.package_ndc
ndc	product	59469-116	openfda.product_ndc
ndc11	package	59469011610	derived:openfda.package_ndc
spl id		78ed18a7-da36-4ead-be28-92693f46c272	id
spl set id		101ff372-e618-4c06-bad1-e2bfbc9e4349	set_id
unii		C9642I91WL	openfda.unii
unii		7C42E2D7B0	openfda.unii
unii		2H1576D5WG	openfda.unii
unii		BDD9991A36	openfda.unii
unii		87EJ76IO83	openfda.unii
unii		5G78C6GB5E	openfda.unii
unii		MK2074187Z	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.