NDC 44911-0500 – Melatonin Pro
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;… · Tablet · Oral
Product NDC44911-0500
Product details
- 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)
- Labeler
- Energique, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketed since
- June 7, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Non-Standardized Plant Allergenic Extract
Active 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
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 44911-0500-1 | 60 TABLET in 1 BOTTLE, PLASTIC (44911-0500-1) | Jun 7, 2019 |