IMMUNOPAR

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:28:32

Label at a glance#

ProductIMMUNOPAR
Active ingredientASTRAGALUS PROPINQUUS ROOT, BAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA WHOLE, GOLDENSEAL, SUS SCROFA LYMPH, SUS SCROFA BONE MARROW, SUS SCROFA NASAL MUCOSA, SUS SCROFA SPLEEN, SUS SCROFA THYMUS, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE, ARSENIC TRIOXIDE, LACHESIS MUTA VENOM, PHOSPHORUS, RANCID BEEF
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 2 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): 9.06% of Hydrastis Canadensis 6X, Lymph Node (SUIS) 6X, Medulla Ossis Suis 6X, Mucosa Nasalis Suis 6X, Spleen (Suis) 6X, Thymus (Suis) 6X, Anas Barbariae,Hepatis ET Cordis Extractum 12X, Arsenicum Album 12X, Lachesis Mutus12X, Phosphorus 12X, Pyrogenium 30X, 0.10% of Astragalus Membranaceus12X, Baptisia Tinctoria 3X, Echinacea (Angustifolia) 3X

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve Painful, irrated throat, mild ear disorders, and minor bronchial irritation with yellow expectoration.**

**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.

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 2 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve Painful, irrated throat, mild ear disorders, and minor bronchial irritation with yellow expectoration.**

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

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

IMMUNOPAR

1 fl. oz. (30 ml)

IMMUNOPARIMMUNOPAR

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
44911-0636-12024-10-28C16284748780-1f386c64a-1b1f-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0636-12023-01-30C16284748780-1f386c64a-1b1f-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0636-1IMMUNOPAR30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0636IMMUNOPAR (ASTRAGALUS MEMBRANACEUS, BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), HYDRASTIS CANADENSIS, LYMPH NODE (SUIS), MEDULLA OSSIS SUIS, MUCOSA NASALIS SUIS, SPLEEN (SUIS), THYMUS (SUIS), ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, ARSENICUM ALBUM, LACHESIS MUTUS, PHOSPHORUS, PYROGENIUM) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20241030_ac04961b-1614-49a2-92d8-28ba283fb7a6.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-063644911-0636-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
IMMUNOPARASTRAGALUS MEMBRANACEUS, BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), HYDRASTIS CANADENSIS, LYMPH NODE (SUIS), MEDULLA OSSIS SUIS, MUCOSA NASALIS SUIS, SPLEEN (SUIS), THYMUS (SUIS), ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, ARSENICUM ALBUM, LACHESIS MUTUS, PHOSPHORUS, PYROGENIUMEnergique, Inc.ac04961b-1614-49a2-92d8-28ba283fb7a62024-10-28WarningsExact identifier
ndc (package): 44911-0636-1
ndc (product): 44911-0636
ndc11 (package): 44911063601
spl id: c888c8fd-5ae9-4c19-a922-5ab49a35e0f0
spl set id: ac04961b-1614-49a2-92d8-28ba283fb7a6

Reported adverse events (FAERS/openFDA)#

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