Hendel Indigestion And Bloating Tablet
FDA Label NDC 62795-1131

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 Hendel Indigestion And Bloating (NDC 62795-1131). 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, uses, active ingredient, inactive ingredient, dosage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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 Indigestion & Bloating 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

Uses

Indigestion & Bloating Relief

For the temporary relief of:
• Indigestion
• Feeling of fullness
• Nausea

Active Ingredient

Each tablet contains equal parts of Carbo vegetabilis 3X; Nux vomica 3X; Argentum nitricum 6X; Arsenicum album 12X; Ipecacuanha 6X

Inactive Ingredient

Lactose, Magnesium stearate

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

* Please review the disclaimer below.