Endoplex F

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: Endoplex F
Generic name: CIMICIFUGA RACEMOSA, FUCUS VESICULOSUS, GLYCYRRHIZA GLABRA, XANTHOXYLUM FRAXINEUM, ADRENALINUM, CEREBRUM SUIS, HYPOPHYSIS SUIS, HYPOTHALAMUS (SUIS), OOPHORINUM (SUIS), PINEAL (SUIS), THYROIDINUM (SUIS), PULSATILLA (VULGARIS), SEPIA
Manufacturer: BioActive Nutritional, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: bfe6d42a-a3e5-44b3-ab8f-b08ad4e2b66f
SPL ID: 83714b9e-4b13-436f-b1c2-f4575cbb81d2
Version: 3
Effective date: 2026-03-30
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:17:03

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Endoplex F	openfda.brand_name
generic name		CIMICIFUGA RACEMOSA, FUCUS VESICULOSUS, GLYCYRRHIZA GLABRA, XANTHOXYLUM FRAXINEUM, ADRENALINUM, CEREBRUM SUIS, HYPOPHYSIS SUIS, HYPOTHALAMUS (SUIS), OOPHORINUM (SUIS), PINEAL (SUIS), THYROIDINUM (SUIS), PULSATILLA (VULGARIS), SEPIA	openfda.generic_name
manufacturer name		BioActive Nutritional, Inc.	openfda.manufacturer_name
ndc	package	43857-0417-1	openfda.package_ndc
ndc	product	43857-0417	openfda.product_ndc
ndc11	package	43857041701	derived:openfda.package_ndc
spl id		83714b9e-4b13-436f-b1c2-f4575cbb81d2	id
spl set id		bfe6d42a-a3e5-44b3-ab8f-b08ad4e2b66f	set_id
unii		6RV024OAUQ	openfda.unii
unii		4GB5DQR532	openfda.unii
unii		2788Z9758H	openfda.unii
unii		A4KL1HMZ7T	openfda.unii
unii		050QZ2EDK7	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		YKH834O4BH	openfda.unii
unii		S7YTV04R8O	openfda.unii
unii		535G2ABX9M	openfda.unii
unii		E8S87O660T	openfda.unii
unii		I76KB35JEV	openfda.unii
unii		K73E24S6X9	openfda.unii
unii		N6R0856Z79	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: If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children . In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Reported adverse events (FAERS/openFDA)#

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