B11 INJUROTOX

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: B11 INJUROTOX
Generic name: ARISTOLOCHIA MILHOMENS, ARNICA MONTANA, ARSENICUM ALBUM, BELLADONNA, BELLIS PERENNIS, BRYONIA, CALENDULA OFFICINALIS, CARBO VEGETABILIS, CHAMOMILLA, CHERRY PLUM FLOWER, CLEMATIS VITALBA FLOWER, ECHINACEA ANGUSTIFOLIA, HAMAMELIS VIRGINIANA, HEPAR SULPHURIS CALCAREUM, HYPERICUM PERFORATUM, IMPATIENS GLANDULIFERA FLOWER, LACHESIS MUTUS, MILLEFOLIUM, PYRENEES STAR OF BETHLEHEM, RHUS TOXICODENDRON, ROCKROSE FLOWER, RUTA GRAVEOLENS, SARCOLACTICUM ACIDUM, SULPHUR IODATUM, SYMPHYTUM OFFICINALE, VERATRUM ALBUM
Manufacturer: Apex Energetics Inc.
Product type: HUMAN OTC DRUG
SPL set ID: baecce61-0514-abe5-e053-2995a90a12a8
SPL ID: 0e768a0e-1c52-7a5b-e063-6394a90a8097
Version: 2
Effective date: 2024-01-08
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 01:28:14

Harmonized routes table
Harmonized routes
SUBLINGUAL

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 · 34 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		B11 INJUROTOX	openfda.brand_name
generic name		ARISTOLOCHIA MILHOMENS, ARNICA MONTANA, ARSENICUM ALBUM, BELLADONNA, BELLIS PERENNIS, BRYONIA, CALENDULA OFFICINALIS, CARBO VEGETABILIS, CHAMOMILLA, CHERRY PLUM FLOWER, CLEMATIS VITALBA FLOWER, ECHINACEA ANGUSTIFOLIA, HAMAMELIS VIRGINIANA, HEPAR SULPHURIS CALCAREUM, HYPERICUM PERFORATUM, IMPATIENS GLANDULIFERA FLOWER, LACHESIS MUTUS, MILLEFOLIUM, PYRENEES STAR OF BETHLEHEM, RHUS TOXICODENDRON, ROCKROSE FLOWER, RUTA GRAVEOLENS, SARCOLACTICUM ACIDUM, SULPHUR IODATUM, SYMPHYTUM OFFICINALE, VERATRUM ALBUM	openfda.generic_name
manufacturer name		Apex Energetics Inc.	openfda.manufacturer_name
ndc	package	63479-0211-1	openfda.package_ndc
ndc	product	63479-0211	openfda.product_ndc
ndc11	package	63479021101	derived:openfda.package_ndc
spl id		0e768a0e-1c52-7a5b-e063-6394a90a8097	id
spl set id		baecce61-0514-abe5-e053-2995a90a12a8	set_id
unii		2P3VWU3H10	openfda.unii
unii		2FXJ6SW4PK	openfda.unii
unii		0KD7R09EAS	openfda.unii
unii		XK4IUX8MNB	openfda.unii
unii		7SCP4N87CI	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		18E7415PXQ	openfda.unii
unii		2HU33I03UY	openfda.unii
unii		CZD6M4PY4B	openfda.unii
unii		N94C2U587S	openfda.unii
unii		F9S9FFU82N	openfda.unii
unii		M9VVZ08EKQ	openfda.unii
unii		R06VWT372T	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		51BRR32WPP	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		VB06AV5US8	openfda.unii
unii		AJU5O1A5ZV	openfda.unii
unii		WQZ3G9PF0H	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		G0R4UBI2ZZ	openfda.unii
unii		QNS6W5US1Z	openfda.unii
unii		L6L8KA2AA0	openfda.unii
unii		T7S323PKJS	openfda.unii
unii		1MBW07J51Q	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

If pregnant or breastfeeding , ask a health professional before use. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if joint pain, bruises, swelling, headache, muscle pain, or other symptoms do not improve within 7 days or are accompanied by fever.

Reported adverse events (FAERS/openFDA)#

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