Dr. Hendel Appetite Control Tablet
FDA Label NDC 62795-1111

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 Appetite Control (NDC 62795-1111). 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, ingredients, inactive ingredient, directions, uses, dr. hendel appetite control, 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 Hendel Appetite Control 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

Appetite Control

Ingredients

Each tablet contains equal parts of Calcarea carbonica 12X; Capsicum annuum 12X; Ferrum metallicum 12X; Fucus vesiculosus 12X; Graphites 12X; Ignatia amara 12X; Lycopodium clavatum 12X

Inactive Ingredient

Lactose, Magnesium stearate

Directions

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:

• Increased or ravenous appetite

• Simple nervous tension

• Feeling of hunger even after a meal

* Please review the disclaimer below.