Drugplain

Melatonin Pro 12 [hp_X]/1

Calcarea Carbonica, Chamomilla, Cocculus Indicus, Coffea Cruda, Ferrum Phosphoricum, Kali Phosphoricum, Magnesia Carbonica, Melatonin, Natrum Muriaticum, Nux Vomica, Pulsatilla (Pratensis) · TABLET · Energique, Inc.

No Recall History
Plain English

Melatonin Pro is an over-the-counter oral tablet that combines melatonin with several homeopathic ingredients and is intended to support sleep. This product is classified as a non-standardized food allergenic extract.

Key Facts

Brand Name
Melatonin Pro
Generic Name
Calcarea Carbonica, Chamomilla, Cocculus Indicus, Coffea Cruda, Ferrum Phosphoricum, Kali Phosphoricum, Magnesia Carbonica, Melatonin, Natrum Muriaticum, Nux Vomica, Pulsatilla (Pratensis)
NDC Code (Product)
44911-0500
Manufacturer
Energique, Inc.
Strength
12 [hp_X]/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Drug Class
Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]
Marketing Start
06/07/2019

Recall History

No Recall History

Frequently Asked Questions

What is Melatonin Pro used for?

Melatonin Pro is an over-the-counter oral tablet that combines melatonin with several homeopathic ingredients and is intended to support sleep. This product is classified as a non-standardized food allergenic extract.

Is Melatonin Pro a controlled substance?

Melatonin Pro is not classified as a controlled substance by the DEA.

What is the generic name for Melatonin Pro?

The generic name for Melatonin Pro is Calcarea Carbonica, Chamomilla, Cocculus Indicus, Coffea Cruda, Ferrum Phosphoricum, Kali Phosphoricum, Magnesia Carbonica, Melatonin, Natrum Muriaticum, Nux Vomica, Pulsatilla (Pratensis). There are no other listed brand versions of Calcarea Carbonica, Chamomilla, Cocculus Indicus, Coffea Cruda, Ferrum Phosphoricum, Kali Phosphoricum, Magnesia Carbonica, Melatonin, Natrum Muriaticum, Nux Vomica, Pulsatilla (Pratensis).

What is the NDC code for Melatonin Pro 12 [hp_X]/1?

The NDC (National Drug Code) for Melatonin Pro 12 [hp_X]/1 is 44911-0500, listed by Energique, Inc..

Product NDC

44911-0500

Package NDC

44911-0500-1

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

Data from openFDA · Public domain (CC0 1.0)