Nerve Pro

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:28:36

Label at a glance#

ProductNerve Pro HP
Active ingredientPLANTAGO MAJOR WHOLE, ZANTHOXYLUM AMERICANUM BARK, CITRULLUS COLOCYNTHIS FRUIT PULP, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, AMANITA MUSCARIA FRUITING BODY, HYPERICUM PERFORATUM WHOLE, SILVER NITRATE, CARBON DISULFIDE, TUBOCURARINE CHLORIDE, THALLIUM
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): 7.14% of Agaricus Muscarius 12X, 30X, 200X, Argentum Nitricum 30X, Carboneum Sulphuratum 30X, Colocynthis 12X, Curare 30X, Hypericum Perforatum 12X, 30X, 200X, Magnesia Phosphorica 12X, Plantago Major 6X, Thallium Metallicum 30X, Xanthoxylum Fraxineum 6X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms of tingling, burning, and numbness in the hands and feet.**

**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

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 symptoms of tingling, burning, and dumbness in the hands and feet.**

**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
NERVE PRO

HP
1 fl. oz. (30 ml)

Nerve Pro HPNerve Pro HP

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0495-12024-10-29C16284748780-1d6a99b39-49f4-a426-e053-dadaa90af4c2DRUG FACTS:
44911-0495-12022-01-28C16284748780-1d6a99b39-49f4-a426-e053-dadaa90af4c2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0495-1Nerve ProHP30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0495NERVE PRO HP (PLANTAGO MAJOR, XANTHOXYLUM FRAXINEUM, COLOCYNTHIS, MAGNESIA PHOSPHORICA, AGARICUS MUSCARIUS, HYPERICUM PERFORATUM, ARGENTUM NITRICUM, CARBONEUM SULPHURATUM, CURARE, THALLIUM METALLICUM) LIQUID [ENERGIQUE, INC.]3Current NDC, Legacy NDC, 1 package rows20241031_846d5805-6f82-4cb4-b64c-adba6d3004e7.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-049544911-0495-1

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

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
Nerve Pro HPPLANTAGO MAJOR, XANTHOXYLUM FRAXINEUM, COLOCYNTHIS, MAGNESIA PHOSPHORICA, AGARICUS MUSCARIUS, HYPERICUM PERFORATUM, ARGENTUM NITRICUM, CARBONEUM SULPHURATUM, CURARE, THALLIUM METALLICUMEnergique, Inc.846d5805-6f82-4cb4-b64c-adba6d3004e72024-10-29WarningsExact identifier
ndc (package): 44911-0495-1
ndc (product): 44911-0495
ndc11 (package): 44911049501
spl id: c98c29e3-90b3-4b1d-8a1d-83f9a70075c6
spl set id: 846d5805-6f82-4cb4-b64c-adba6d3004e7

Reported adverse events (FAERS/openFDA)#

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