Dr. Hendel Back Pain Relief Tablet
FDA Label NDC 62795-1114

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Medinatura Inc for the product Dr. Hendel Back Pain Relief (NDC 62795-1114). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding warnings, keep out of reach of children, indications, active ingredient, inactive ingredient, directions, uses, dr. hendel back pain relief, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Warnings

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

KEEP OUT OF REACH OF CHILDREN

Indications

Back Pain Relief

Active Ingredient

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

Lactose, Magnesium stearate

Directions

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

For the temporary relief of:

  • Shoulder, back & hip pain

  • Aches & stiffness in back muscles

  • Back spasms and cramps

* Please review the disclaimer below.