Dr. Hendel Back Pain Relief

Manufacturer
MediNatura Inc
Effective date
2022-08-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:18:02

Label at a glance#

ProductDr. Hendel Back Pain Relief
Active ingredientHORSE CHESTNUT, BRYONIA ALBA ROOT, CITRULLUS COLOCYNTHIS FRUIT PULP, SOLANUM DULCAMARA TOP, PSEUDOGNAPHALIUM OBTUSIFOLIUM, HYPERICUM PERFORATUM, STRYCHNOS NUX-VOMICA SEED, TOXICODENDRON PUBESCENS LEAF
Label structure8 sections

Indications and uses

For the temporary relief of: Shoulder, back & hip pain Aches & stiffness in back muscles Back spasms and cramps

Dosage and administration

Dosage: Adults 18 and over : 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician.

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 Hendel Back Pain Relief or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS

OTC - PURPOSE SECTION

Back Pain Relief

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Each tablet containsequal parts of: Aesculus hippocastanum 6X; Bryonia 6X; Colocynthis 6X; Dulcamara 6X; Gnaphalium polycephalum 6X; Hypericum perforatum 6X; Nux vomica 6X; Rhus tox 12X

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Lactose, Magnesium stearate

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Dosage: Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician.

USES

INDICATIONS & USAGE SECTION

For the temporary relief of:

  • Shoulder, back & hip pain

  • Aches & stiffness in back muscles

  • Back spasms and cramps

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dr. Hendel Back Pain ReliefDr. Hendel Back Pain Relief

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62795-1114-2Dr. Hendel Back Pain Relief100 in 1 BOTTLETABLET1003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62795-1114DR. HENDEL BACK PAIN RELIEF (HORSE CHESTNUT, BRYONIA ALBA ROOT, CITRULLUS COLOCYNTHIS FRUIT PULP, SOLANUM DULCAMARA TOP, PSEUDOGNAPHALIUM OBTUSIFOLIUM, HYPERICUM PERFORATUM, STRYCHNOS NUX-VOMICA SEED, AND TOXICODENDRON PUBESCENS LEAF) TABLET [MEDINATURA INC]3Current NDC, Legacy NDC, 1 package rows20220820_df7c5fb6-9d23-49af-a273-bb123e7f95d4.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62795-1114-2EA - Each62795-1114852a09f6-52b9-4394-9db8-70ce3ef0a02912017-04-05

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62795-111462795-1114-2

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

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
Dr. Hendel Back Pain ReliefHORSE CHESTNUT, BRYONIA ALBA ROOT, CITRULLUS COLOCYNTHIS FRUIT PULP, SOLANUM DULCAMARA TOP, PSEUDOGNAPHALIUM OBTUSIFOLIUM, HYPERICUM PERFORATUM, STRYCHNOS NUX-VOMICA SEED, AND TOXICODENDRON PUBESCENS LEAFMediNatura Incdf7c5fb6-9d23-49af-a273-bb123e7f95d42022-08-18WarningsExact identifier
ndc (package): 62795-1114-2
ndc (product): 62795-1114
ndc11 (package): 62795111402
spl id: a0d1f708-8647-44fa-839c-44f8fa9a6db3
spl set id: df7c5fb6-9d23-49af-a273-bb123e7f95d4

Reported adverse events (FAERS/openFDA)#

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