Hevert Detox Intestinum

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 Intestinum
Generic name: EICHHORNIA CRASSIPES WHOLE, OKOUBAKA AUBREVILLEI BARK, QUASSIA AMARA WOOD, AND TARAXACUM OFFICINALE
Manufacturer: Hevert Arzneimittel GmbH & Co KG
Product type: HUMAN OTC DRUG
SPL set ID: 6c07bbb5-7770-4ab1-b336-00703e949fc9
SPL ID: 5fd4ef4b-cf67-4828-8492-266a585109a6
Version: 4
Effective date: 2022-11-30
Source export date: 2026-10-12
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:24:03

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Hevert Detox Intestinum	openfda.brand_name
generic name		EICHHORNIA CRASSIPES WHOLE, OKOUBAKA AUBREVILLEI BARK, QUASSIA AMARA WOOD, AND TARAXACUM OFFICINALE	openfda.generic_name
manufacturer name		Hevert Arzneimittel GmbH & Co KG	openfda.manufacturer_name
ndc	package	54532-0031-5	openfda.package_ndc
ndc	product	54532-0031	openfda.product_ndc
ndc11	package	54532003105	derived:openfda.package_ndc
spl id		5fd4ef4b-cf67-4828-8492-266a585109a6	id
spl set id		6c07bbb5-7770-4ab1-b336-00703e949fc9	set_id
unii		S5249Q85HW	openfda.unii
unii		39981FM375	openfda.unii
unii		216V7S21BH	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

Warnings For oral use only. Stop use and ask a doctor if symptoms persist for more than 7 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.