FDA.reportPublic FDA data

Numbness HP

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:28:33

Label at a glance#

ProductNumbness HP
Active ingredientACONITUM NAPELLUS WHOLE, AMANITA MUSCARIA FRUITING BODY, ONION, ARNICA MONTANA WHOLE, ARABICA COFFEE BEAN, HYPERICUM PERFORATUM WHOLE, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLUBILIS, PHOSPHORUS, LEAD
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 Aconitum Napellus 30X, Agaricus Muscarius 30X, Allium Cepa 30X, Arnica Montana 30X, Coffea Cruda 30X, Hypericum Perforatum 30X, Lycopodium Clavatum 30X, Mercurius Solubilis 30X, Phosphorus 30X, Plumbum Metallicum 30X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms of numbness, tingling, and irritation of nerves.**

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

WARNING:

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 symptoms of numbness, tingling, and irritation of nerves.**

**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

NUMBNESS HP

1 fl. oz. (30 ml)

NUMBNESS HPNUMBNESS HP

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0625-12024-10-29C16284748780-1f386c649-c79b-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0625-12023-01-30C16284748780-1f386c649-c79b-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0625-1Numbness HP30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0625NUMBNESS HP (ACONITUM NAPELLUS, AGARICUS MUSCARIUS, ALLIUM CEPA, ARNICA MONTANA, COFFEA CRUDA, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, PHOSPHORUS, PLUMBUM METALLICUM) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20241031_0c4ba547-b4b4-41d0-8a6b-1141ff5f9453.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-062544911-0625-1

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
ACONITUM NAPELLUS WHOLEU0NQ8555JDACTIB
AMANITA MUSCARIA FRUITING BODYDIF093I037ACTIB
ONION492225Q21HACTIB
ARNICA MONTANA WHOLEO80TY208ZWACTIB
ARABICA COFFEE BEAN3SW678MX72ACTIB
HYPERICUM PERFORATUM WHOLEXK4IUX8MNBACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
MERCURIUS SOLUBILIS324Y4038G2ACTIB
PHOSPHORUS27YLU75U4WACTIB
LEAD2P299V784PACTIB
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
Numbness HPACONITUM NAPELLUS, AGARICUS MUSCARIUS, ALLIUM CEPA, ARNICA MONTANA, COFFEA CRUDA, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, PHOSPHORUS, PLUMBUM METALLICUMEnergique, Inc.0c4ba547-b4b4-41d0-8a6b-1141ff5f94532024-10-29WarningsExact identifier
ndc (package): 44911-0625-1
ndc (product): 44911-0625
ndc11 (package): 44911062501
spl id: 9aec25cf-ef9c-417f-b225-db8a2a20306d
spl set id: 0c4ba547-b4b4-41d0-8a6b-1141ff5f9453

Reported adverse events (FAERS/openFDA)#

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