FDA.reportPublic FDA data

Hendel Nerve Pain Relief

Manufacturer
MediNatura Inc
Effective date
2023-02-16
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:20:05

Label at a glance#

ProductHendel Nerve Pain Relief
Active ingredientDAPHNE MEZEREUM BARK, ARNICA MONTANA, ARSENIC TRIOXIDE, ATROPA BELLADONNA, TOXICODENDRON PUBESCENS LEAF, CITRULLUS COLOCYNTHIS FRUIT PULP, PSEUDOGNAPHALIUM OBTUSIFOLIUM, HYPERICUM PERFORATUM, RUTA GRAVEOLENS FLOWERING TOP
Label structure8 sections

Indications and uses

For the temporary relief of: • Tingling sensation • Shooting pain

Dosage and administration

Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician. If symptoms persist, take 1 tablet every hour; not to exceed 12 tablets daily.

Label contents#

Full prescribing information#

WARNINGS

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if sensitivity to Nerve Pain Relief or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately.

SPL UNCLASSIFIED SECTION

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

PURPOSE

OTC - PURPOSE SECTION

Nerve Pain Relief

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Each tablet contains equal parts of Mezereum 3X; Arnica montana 6X; Arsenicum album 12X; Belladonna 6X; Colocynthis 6X; Gnaphalium polycephalum 6X; Hypericum perforatum 6X; Ruta graveolens 6X; Rhux tox 12X

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Lactose, Magnesium stearate

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician. If symptoms persist, take 1 tablet every hour; not to exceed 12 tablets daily.

USES

INDICATIONS & USAGE SECTION

For the temporary relief of:
• Tingling sensation
• Shooting pain

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62795-1132-2Hendel Nerve Pain Relief100 in 1 BOTTLETABLET1004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62795-1132HENDEL NERVE PAIN RELIEF (DAPHNE MEZEREUM BARK, ARNICA MONTANA, ARSENIC TRIOXIDE, ATROPA BELLADONNA, CITRULLUS COLOCYNTHIS FRUIT PULP, PSEUDOGNAPHALIUM OBTUSIFOLIUM, HYPERICUM PERFORATUM, RUTA GRAVEOLENS FLOWERING TOP, AND TOXICODENDRON PUBESCENS LEAF) TABLET [MEDINATURA INC]4Legacy NDC, 1 package rows20230217_e50188f2-b437-48e3-8aec-186b31fabf8d.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62795-1132-2EA - Each62795-11323dc04499-478d-424a-bef9-839b0ce5400a12022-07-06

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62795-113262795-1132-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
DAPHNE MEZEREUM BARKX2N6E405GVACTIB
ARNICA MONTANAO80TY208ZWACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
CITRULLUS COLOCYNTHIS FRUIT PULP23H32AOH17ACTIB
PSEUDOGNAPHALIUM OBTUSIFOLIUM36XQ854NWWACTIB
HYPERICUM PERFORATUMXK4IUX8MNBACTIB
RUTA GRAVEOLENS FLOWERING TOPN94C2U587SACTIB
MAGNESIUM STEARATE70097M6I30IACT
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT

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
acec53a2-5fcb-46aa-9a68-45bdb26a1e06e50188f2-b437-48e3-8aec-186b31fabf8d2023-02-16WarningsExact identifier
spl id: acec53a2-5fcb-46aa-9a68-45bdb26a1e06
spl set id: e50188f2-b437-48e3-8aec-186b31fabf8d

Reported adverse events (FAERS/openFDA)#

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