Neuropar

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-29
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:28:35

Label at a glance#

ProductNeuropar
Active ingredientPASSIFLORA INCARNATA FLOWERING TOP, SUS SCROFA ADRENAL GLAND, THYROID, BOVINE, ARANEUS DIADEMATUS, ARNICA MONTANA WHOLE, ARSENIC TRIOXIDE, HYPERICUM PERFORATUM WHOLE, LACHESIS MUTA VENOM, PHYSOSTIGMA VENENOSUM SEED, ZINC PICRATE NONAHYDRATE
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): 12.48% of Aranea Diadema 12X, Arnica Montana 12X, Arsenicum Album 12X, Glandula Suprarenalis Suis 6X, Hypericum Perforatum 12X, Lachesis Mutus 12X, Physostigma Venenosum 15X, Zincum Picricum 15X; 0.10% of Passiflora Incarnata 3X, Thyroidinum (Bovine) 6X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve numbness and tingling, stiffness in nape of the neck with shooting pain, and tingling and burning pain with numbness.**

**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

Keep out of reach of children. 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 numbness and tingling, stiffness in nape of the neck with shooting pain, and tingling and burning pain with numbness.**

**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
NEUROPAR
1 fl. oz. (30 ml)

NeuroparNeuropar

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0251-12024-10-29C16284748780-1ba0f9c33-2791-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0251-12023-01-30C16284748780-1ba0f9c33-2791-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0251-12021-04-12C16284748780-1ba0f9c33-2791-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0251-12021-01-29C16284748780-1ba0f9c33-2791-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0251-1Neuropar30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0251NEUROPAR (PASSIFLORA INCARNATA, GLANDULA SUPRARENALIS SUIS, THYROIDINUM (BOVINE), ARANEA DIADEMA, ARNICA MONTANA, ARSENICUM ALBUM, HYPERICUM PERFORATUM, LACHESIS MUTUS, PHYSOSTIGMA VENENOSUM, ZINCUM PICRICUM) LIQUID [ENERGIQUE, INC.]4Current NDC, Legacy NDC, 1 package rows20241031_76fc7c3d-c001-4ba0-821b-7d8544f6670b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARANEUS DIADEMATUSACTIVE INGREDIENT6T6CO7R3Z51
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZW1
ARSENIC TRIOXIDEACTIVE INGREDIENTS7V92P67HO1
HYPERICUM PERFORATUMACTIVE INGREDIENTXK4IUX8MNB1
LACHESIS MUTA VENOMACTIVE INGREDIENTVSW71SS07I1
PASSIFLORA INCARNATA FLOWERING TOPACTIVE INGREDIENTCLF5YFS11O1
PHYSOSTIGMA VENENOSUM SEEDACTIVE INGREDIENTCJV9E9IIOA1
SUS SCROFA ADRENAL GLANDACTIVE INGREDIENT398IYQ16YV1
THYROID, BOVINEACTIVE INGREDIENTMN18OTN73W1
ZINC PICRATE NONAHYDRATEACTIVE INGREDIENT0057VRD75N1
ARANEUS DIADEMATUSACTIVE MOIETY6T6CO7R3Z51
ARNICA MONTANAACTIVE MOIETYO80TY208ZW1
ARSENIC CATION (3+)ACTIVE MOIETYC96613F5AV1
HYPERICUM PERFORATUMACTIVE MOIETYXK4IUX8MNB1
LACHESIS MUTA VENOMACTIVE MOIETYVSW71SS07I1
PASSIFLORA INCARNATA FLOWERING TOPACTIVE MOIETYCLF5YFS11O1
PHYSOSTIGMA VENENOSUM SEEDACTIVE MOIETYCJV9E9IIOA1
SUS SCROFA ADRENAL GLANDACTIVE MOIETY398IYQ16YV1
THYROID, BOVINEACTIVE MOIETYMN18OTN73W1
ZINC CATIONACTIVE MOIETY13S1S8SF371
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-025144911-0251-1

Ingredients#

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

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

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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
NeuroparPASSIFLORA INCARNATA, GLANDULA SUPRARENALIS SUIS, THYROIDINUM (BOVINE), ARANEA DIADEMA, ARNICA MONTANA, ARSENICUM ALBUM, HYPERICUM PERFORATUM, LACHESIS MUTUS, PHYSOSTIGMA VENENOSUM, ZINCUM PICRICUMEnergique, Inc.76fc7c3d-c001-4ba0-821b-7d8544f6670b2024-10-29WarningsExact identifier
ndc (package): 44911-0251-1
ndc (product): 44911-0251
ndc11 (package): 44911025101
spl id: cdb53b5c-1fc6-426e-82e7-bbaf3f1b1598
spl set id: 76fc7c3d-c001-4ba0-821b-7d8544f6670b

Reported adverse events (FAERS/openFDA)#

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