Neuralgia

Manufacturer
BioActive Nutritional, Inc. | Apotheca Company
Effective date
2026-03-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:38:02

Label at a glance#

ProductNeuralgia HP
Active ingredientAMANITA MUSCARIA FRUITING BODY, ONION, ARNICA MONTANA WHOLE, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLUBILIS, PHOSPHORUS, LEAD
Label structure9 sections

Indications and uses

For temporary relief of symptoms of numbness, tingling, muscle cramps, and nerve pain.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage and administration

• 10 drops orally, 3 times a day or as directed by a health care professional. • Consult a health care professional for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Agaricus Muscarius 30X, Allium Cepa 30X, Arnica Montana 30X, Hypericum Perforatum 30X, Lycopodium Clavatum 30X, Mercurius Solubilis 30X, Phosphorus 30X, Plumbum Metallicum 30X.

PURPOSE:

OTC - PURPOSE SECTION

Agaricus Muscarius – spasming of muscles,** Allium Cepa - antioxidant,** Arnica Montana – anti-inflammatory,** Hypericum Perforatum – shooting pain,** Lycopodium Clavatum – tingling and numbness,** Mercurius Solubilis – anti-inflammatory,** Phosphorus – fatigue, weakness,** Plumbum Metallicum – numbness**

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

USES:

INDICATIONS & USAGE SECTION

For temporary relief of symptoms of numbness, tingling, muscle cramps, and nerve pain.**

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

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health care 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

• 10 drops orally, 3 times a day or as directed by a health care professional.

• Consult a health care professional for use in children under 12 years of age.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Distributed by:

BioActive Nutritional, Inc.

1803 N. Wickham Rd.

Melbourne, FL 32935

bioactivenutritional.com

1-800-288-9525

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BioActive Nutritional

NEURALGIA HP

HOMEOPATHIC

1 fl. oz. (30 mL)

NEURALGIA HPNEURALGIA HP

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130210184341695GTIN-13: 0210184341695
EAN-13: 0210184341695
GTIN-12: 210184341695
UPC-A: 210184341695
GTIN storage (14 digits): 00210184341695
BANI0288 Neuralgia HP 1-27-26.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43857-0381-1NeuralgiaHP30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AMANITA MUSCARIA FRUITING BODYACTIVE INGREDIENTDIF093I0372
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZW2
HYPERICUM PERFORATUMACTIVE INGREDIENTXK4IUX8MNB2
LEADACTIVE INGREDIENT2P299V784P2
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4792
MERCURIUS SOLUBILISACTIVE INGREDIENT324Y4038G22
ONIONACTIVE INGREDIENT492225Q21H2
PHOSPHORUSACTIVE INGREDIENT27YLU75U4W2
AMANITA MUSCARIA FRUITING BODYACTIVE MOIETYDIF093I0372
ARNICA MONTANAACTIVE MOIETYO80TY208ZW2
HYPERICUM PERFORATUMACTIVE MOIETYXK4IUX8MNB2
LEADACTIVE MOIETY2P299V784P2
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4792
MERCURIUS SOLUBILISACTIVE MOIETY324Y4038G22
ONIONACTIVE MOIETY492225Q21H2
PHOSPHORUSACTIVE MOIETY27YLU75U4W2
ALCOHOLINACTIVE INGREDIENT3K9958V90M2
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43857-038143857-0381-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
Neuralgia HPAGARICUS MUSCARIUS, ALLIUM CEPA, ARNICA MONTANA, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, PHOSPHORUS, PLUMBUM METALLICUMBioActive Nutritional, Inc.9674fbbb-ab2d-412e-bf69-3bd7b6b0134b2026-03-17WarningsExact identifier
ndc (package): 43857-0381-1
ndc (product): 43857-0381
ndc11 (package): 43857038101
spl id: 7f89953f-716e-4ffc-8e5d-880d0e3aa482
spl set id: 9674fbbb-ab2d-412e-bf69-3bd7b6b0134b

Reported adverse events (FAERS/openFDA)#

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