FDA.reportPublic FDA data

Joint HP

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 02:26:30

Label at a glance#

ProductJoint HP
Active ingredientAPIS MELLIFERA, BRYONIA ALBA ROOT, CAUSTICUM, COLCHICUM AUTUMNALE BULB, POTASSIUM CARBONATE, KALMIA LATIFOLIA LEAF, LEDUM PALUSTRE TWIG, PULSATILLA PRATENSIS WHOLE, 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 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): 10% of Apis Mellifica 30X, Bryonia (Alba) 30X, Causticum 30X, Colchicum Autumnale 30X, Kali Carbonicum 30X, Kalmia Latifolia 30X, Ledum Palustre 30X, Pulsatilla (Pratensis) 30X, Rhododendron Chrysanthum 30X, Rhus Tox 30X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms due to minor joint inflammation and swelling.**

**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 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 due to minor joint inflammation and swelling.**

**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

JOINT HP

1 fl. oz. (30 ml)

Joint HPJoint HP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0585-12024-03-26C16284748780-1f386c64a-2eb1-0266-e053-dadaa90a7c1aDRUG FACTS;
44911-0585-12023-01-30C16284748780-1f386c64a-2eb1-0266-e053-dadaa90a7c1aDRUG FACTS;

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0585-1Joint HP30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0585JOINT HP (APIS MELLIFICA, BRYONIA (ALBA), CAUSTICUM, COLCHICUM AUTUMNALE, KALI CARBONICUM, KALMIA LATIFOLIA, LEDUM PALUSTRE, PULSATILLA (PRATENSIS), RHODODENDRON CHRYSANTHUM, RHUS TOX) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20240328_f65bb6ac-3482-47b1-a678-eff4d130aea1.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-058544911-0585-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
APIS MELLIFERA7S82P3R43ZACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
CAUSTICUMDD5FO1WKFUACTIB
COLCHICUM AUTUMNALE BULB993QHL78E6ACTIB
POTASSIUM CARBONATEBQN1B9B9HAACTIB
KALMIA LATIFOLIA LEAF79N6542N18ACTIB
LEDUM PALUSTRE TWIG877L01IZ0PACTIB
PULSATILLA PRATENSIS WHOLE8E272251DIACTIB
RHODODENDRON AUREUM LEAFIV92NQJ73UACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
Joint HPAPIS MELLIFICA, BRYONIA (ALBA), CAUSTICUM, COLCHICUM AUTUMNALE, KALI CARBONICUM, KALMIA LATIFOLIA, LEDUM PALUSTRE, PULSATILLA (PRATENSIS), RHODODENDRON CHRYSANTHUM, RHUS TOXEnergique, Inc.f65bb6ac-3482-47b1-a678-eff4d130aea12024-03-26WarningsExact identifier
ndc (package): 44911-0585-1
ndc (product): 44911-0585
ndc11 (package): 44911058501
spl id: f462574f-a238-4632-a595-e1a3e6afb0f0
spl set id: f65bb6ac-3482-47b1-a678-eff4d130aea1

Reported adverse events (FAERS/openFDA)#

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