Hevert Detox Kidney

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: Hevert Detox Kidney
Generic name: NITRIC ACID, APIS MELLIFERA, ATROPA BELLADONNA, LYTTA VESICATORIA, JUNIPER BERRY, AND SOLIDAGO VIRGAUREA FLOWERING TOP
Manufacturer: Hevert Arzneimittel GmbH & Co KG
Product type: HUMAN OTC DRUG
SPL set ID: cfad4864-7b02-4389-82f1-49669b651b48
SPL ID: 01fabd3b-07af-43df-9faf-5476d53a30a9
Version: 6
Effective date: 2022-12-01
Source export date: 2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:29:13

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Hevert Detox Kidney	openfda.brand_name
generic name		NITRIC ACID, APIS MELLIFERA, ATROPA BELLADONNA, LYTTA VESICATORIA, JUNIPER BERRY, AND SOLIDAGO VIRGAUREA FLOWERING TOP	openfda.generic_name
manufacturer name		Hevert Arzneimittel GmbH & Co KG	openfda.manufacturer_name
ndc	package	54532-0032-5	openfda.package_ndc
ndc	product	54532-0032	openfda.product_ndc
ndc11	package	54532003205	derived:openfda.package_ndc
spl id		01fabd3b-07af-43df-9faf-5476d53a30a9	id
spl set id		cfad4864-7b02-4389-82f1-49669b651b48	set_id
unii		411VRN1TV4	openfda.unii
unii		3Q034RO3BT	openfda.unii
unii		WQZ3G9PF0H	openfda.unii
unii		O84B5194RL	openfda.unii
unii		7S82P3R43Z	openfda.unii
unii		5405K23S50	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 oral use only. Blood in urine, fever, nausea, vomiting, pain in kidney area or acute urinary retention may be serious. Consult a doctor promptly if any of these symptoms occur. Do not use if you are allergic to bee venom Stop use and ask a doctor if symptoms persist for more than 5 days, worsen or new symptoms occur. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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