A03 ULTRA ANTITOX

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: A03 ULTRA ANTITOX
Generic name: ALFALFA, AMERICAN GINSENG, APIS MELLIFICA, ASPARAGUS OFFICINALIS, AVENA SATIVA, BARYTA IODATA, BERBERIS VULGARIS, BRYONIA, CARDUUS MARIANUS, CHAMOMILLA, CHELIDONIUM MAJUS, CONIUM MACULATUM, FERRUM IODATUM, LAPIS ALBUS, LYCOPODIUM CLAVATUM, NATRUM CARBONICUM, PASSIFLORA INCARNATA, SCROPHULARIA NODOSA, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE, UVA URSI
Manufacturer: Apex Energetics Inc.
Product type: HUMAN OTC DRUG
SPL set ID: b945cb81-aee4-38e8-e053-2a95a90aa8df
SPL ID: 0e765c65-dfc5-b0fa-e063-6294a90a4b51
Version: 2
Effective date: 2024-01-08
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:18:02

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 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		A03 ULTRA ANTITOX	openfda.brand_name
generic name		ALFALFA, AMERICAN GINSENG, APIS MELLIFICA, ASPARAGUS OFFICINALIS, AVENA SATIVA, BARYTA IODATA, BERBERIS VULGARIS, BRYONIA, CARDUUS MARIANUS, CHAMOMILLA, CHELIDONIUM MAJUS, CONIUM MACULATUM, FERRUM IODATUM, LAPIS ALBUS, LYCOPODIUM CLAVATUM, NATRUM CARBONICUM, PASSIFLORA INCARNATA, SCROPHULARIA NODOSA, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE, UVA URSI	openfda.generic_name
manufacturer name		Apex Energetics Inc.	openfda.manufacturer_name
ndc	package	63479-0103-1	openfda.package_ndc
ndc	product	63479-0103	openfda.product_ndc
ndc11	package	63479010301	derived:openfda.package_ndc
spl id		0e765c65-dfc5-b0fa-e063-6294a90a4b51	id
spl set id		b945cb81-aee4-38e8-e053-2a95a90aa8df	set_id
unii		7E889U5RNN	openfda.unii
unii		8W75VCV53Q	openfda.unii
unii		DJO934BRBD	openfda.unii
unii		Z1EJP3037Z	openfda.unii
unii		Q28R5GF371	openfda.unii
unii		1TH8Q20J0U	openfda.unii
unii		39981FM375	openfda.unii
unii		U946SH95EE	openfda.unii
unii		WKC4T7680A	openfda.unii
unii		2NVP93XVQ3	openfda.unii
unii		3M5V3D1X36	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		MA9CQJ3F7F	openfda.unii
unii		45P3261C7T	openfda.unii
unii		7S82P3R43Z	openfda.unii
unii		CLF5YFS11O	openfda.unii
unii		5405K23S50	openfda.unii
unii		G0R4UBI2ZZ	openfda.unii
unii		C88X29Y479	openfda.unii
unii		F5452U54PN	openfda.unii
unii		7H443NUB2T	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 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 fatigue, headache, muscle aches and cramps, irritability, water retention, sadness, 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.