United States · FDA National Drug Code directory

Melatonin Pro

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
44911-0500_bdfbe914-ba46-48a2-885f-a5c8b74c8f7b
Product NDC
44911-0500
Form
TABLET
Composition / generic term
Calcarea Carbonica, Chamomilla, Cocculus Indicus, Coffea Cruda, Ferrum Phosphoricum, Kali Phosphoricum, Magnesia Carbonica, Melatonin, Natrum Muriaticum, Nux Vomica, Pulsatilla (Pratensis)
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20190607
Source listing expiry
20261231

Source-listed ingredients

  • OYSTER SHELL CALCIUM CARBONATE, CRUDE — 12 [hp_X]/1
  • MATRICARIA CHAMOMILLA — 12 [hp_X]/1
  • ANAMIRTA COCCULUS SEED — 12 [hp_X]/1
  • ARABICA COFFEE BEAN — 12 [hp_X]/1
  • FERROSOFERRIC PHOSPHATE — 12 [hp_X]/1
  • DIBASIC POTASSIUM PHOSPHATE — 12 [hp_X]/1
  • MAGNESIUM CARBONATE — 12 [hp_X]/1
  • MELATONIN — 12 [hp_X]/1
  • SODIUM CHLORIDE — 12 [hp_X]/1
  • STRYCHNOS NUX-VOMICA SEED — 12 [hp_X]/1
  • PULSATILLA PRATENSIS WHOLE — 12 [hp_X]/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET in 1 BOTTLE, PLASTIC (44911-0500-1) · 44911-0500-1

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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