DRUG FACTS:

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2026-07-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-08-04 03:32:25

Label at a glance#

ProductJointox BB
Active ingredientBAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA WHOLE, GOLDENSEAL, BORRELIA BURGDORFERI, BABESIA MICROTI, EHRLICHIA CANIS, HEPATITIS B VIRUS, NEISSERIA MENINGITIDIS, ARSENIC TRIOXIDE, BRYONIA ALBA ROOT, CHELIDONIUM MAJUS WHOLE, COLCHICUM AUTUMNALE BULB, KALMIA LATIFOLIA LEAF, LEDUM PALUSTRE TWIG, LYCOPODIUM CLAVATUM SPORE, PHOSPHORUS, 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 for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 4.75% of Arsenicum Album 30C, Babesia Microti 20X, 200X, Borrelia Burgdorferi Nosode 12X, 30X, 200X, Bryonia (Alba) 30C, Chelidonium Majus 30C, Colchicum Autumnale 30C, Ehrlichia Nosode (Canine) 20X, 200X, Hepatitis B Nosode 30X, 200X, Hydrastis Canadensis 6X, Kalmia Latifolia 30C, Ledum Palustre 30C, Lycopodium Clavatum 30C, Meningococcus Nosode 30X, 200X, Phosphorus 30C, Rhus Tox 30C; 0.10% Baptisia Tinctoria 3X, Echinacea (Angustifolia) 3X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with infections, such as aches and pains of joints and muscles.**

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

WARNINGS:

WARNINGS SECTION

If pregnant or breastfeeding, 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 for more than 7 days, 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 associated with infections, such as aches and pains of joints and muscles.**

**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 BB

4fl. oz. (120 ml)

JOINTOX BBJOINTOX BB

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0644-12024-07-16C16284748780-1f386c64a-36d2-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0644-12024-07-16C16284748780-1f386c64a-36d2-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0644-12023-01-30C16284748780-1f386c64a-36d2-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0644-12023-01-30C16284748780-1f386c64a-36d2-0266-e053-dadaa90a7c1aDRUG FACTS:

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-064444911-0644-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-07-12full-release2026-06-01 02:27:32

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 BBBAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), HYDRASTIS CANADENSIS, BORRELIA BURGDORFERI NOSODE, BABESIA MICROTI, EHRLICHIA NOSODE (CANINE), HEPATITIS B NOSODE, MENINGOCOCCUS NOSODE, ARSENICUM ALBUM, BRYONIA (ALBA), CHELIDONIUM MAJUS, COLCHICUM AUTUMNALE, KALMIA LATIFOLIA, LEDUM PALUSTRE, LYCOPODIUM CLAVATUM, PHOSPHORUS, RHUS TOXEnergique, Inc.acb949d3-1def-4a17-a159-a79614b8f77d2026-07-31WarningsExact identifier
ndc (package): 44911-0644-1
ndc (product): 44911-0644
ndc11 (package): 44911064401
spl id: 089b14a5-f28c-4298-8621-5816c298a867
spl set id: acb949d3-1def-4a17-a159-a79614b8f77d

Reported adverse events (FAERS/openFDA)#

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