Drugplain

Mentox HP 30 [hp_X]/mL

Aurum Metallicum, Baryta Carbonica, Calcarea Carbonica, Lachesis Mutus, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Phosphorus · LIQUID · Energique, Inc.

No Recall History
Plain English

Mentox HP is a liquid containing aurum metallicum, baryta carbonica, calcarea carbonica, lachesis mutus, lycopodium clavatum, natrum muriaticum, nux vomica, phosphorus at 30 [hp_X]/mL, taken oral. Manufactured by Energique, Inc..

Key Facts

Brand Name
Mentox HP
Generic Name
Aurum Metallicum, Baryta Carbonica, Calcarea Carbonica, Lachesis Mutus, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Phosphorus
NDC Code (Product)
44911-0299
Manufacturer
Energique, Inc.
Strength
30 [hp_X]/mL
Dosage Form
LIQUID
Route
ORAL
Marketing Status
Drug Class
Standardized Chemical Allergen [EPC]; Non-Standardized Plant Allergenic Extract [EPC]
Marketing Start
11/18/2015

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

INDICATIONS: May temporarily relieve mental confusion, forgetfulness, and tendency toward melancholy.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage & Administration

DIRECTIONS: Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Warnings

WARNINGS: If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Frequently Asked Questions

What is Mentox HP used for?

Mentox HP contains Aurum Metallicum, Baryta Carbonica, Calcarea Carbonica, Lachesis Mutus, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Phosphorus. It is a liquid taken oral. Consult your doctor for specific uses.

Is Mentox HP a controlled substance?

Mentox HP is not classified as a controlled substance by the DEA.

What is the generic name for Mentox HP?

The generic name for Mentox HP is Aurum Metallicum, Baryta Carbonica, Calcarea Carbonica, Lachesis Mutus, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Phosphorus. There are no other listed brand versions of Aurum Metallicum, Baryta Carbonica, Calcarea Carbonica, Lachesis Mutus, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Phosphorus.

What is the NDC code for Mentox HP 30 [hp_X]/mL?

The NDC (National Drug Code) for Mentox HP 30 [hp_X]/mL is 44911-0299, listed by Energique, Inc..

Product NDC

44911-0299

Package NDC

44911-0299-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)