Jointox AI

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-03-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:26:28

Label at a glance#

ProductJointox AI
Active ingredientBRYONIA ALBA ROOT, COLCHICUM AUTUMNALE BULB, FORMICA RUFA, KALMIA LATIFOLIA LEAF, LEDUM PALUSTRE TWIG, LYCOPODIUM CLAVATUM SPORE, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 12.50% of Bryonia (Alba) 30X, Colchicum Autumnale 30X, Formica Rufa 30X, Kalmia Latifolia 30X, Ledum Palustre 30X, Lycopodium Clavatum 30X, Rhododendron Chrysanthum 30X, Rhus Tox 30X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms due to joint aches and pains, swelling, and gout.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

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.

Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms due to joint aches and pains, swelling, and gout.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579 800.869.8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

JOINTOX AI

1 fl. oz. (30 ml)

JOINTOX AIJOINTOX AI

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0586-12024-03-26C16284748780-1f386c649-b2f6-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0586-12023-01-30C16284748780-1f386c649-b2f6-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0586-1Jointox AI30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0586JOINTOX AI (BRYONIA (ALBA), COLCHICUM AUTUMNALE, FORMICA RUFA, KALMIA LATIFOLIA, LEDUM PALUSTRE, LYCOPODIUM CLAVATUM, RHODODENDRON CHRYSANTHUM, RHUS TOX) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20240328_691a5899-de6c-4a4f-87a2-b338519b8474.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-058644911-0586-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Jointox AIBRYONIA (ALBA), COLCHICUM AUTUMNALE, FORMICA RUFA, KALMIA LATIFOLIA, LEDUM PALUSTRE, LYCOPODIUM CLAVATUM, RHODODENDRON CHRYSANTHUM, RHUS TOXEnergique, Inc.691a5899-de6c-4a4f-87a2-b338519b84742024-03-26WarningsExact identifier
ndc (package): 44911-0586-1
ndc (product): 44911-0586
ndc11 (package): 44911058601
spl id: 17238719-3688-4140-b872-1330903a755f
spl set id: 691a5899-de6c-4a4f-87a2-b338519b8474

Reported adverse events (FAERS/openFDA)#

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