Melatonin Pro
- Product NDC
- 44911-0491
- 11-digit product format
- 449110491
- Labeler code
- 44911
- Product ID
- 44911-0491_0ea9a1fd-e7b3-4b85-b1d5-bb35858cd231
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcarea Carbonica, Chamomilla, Cocculus Indicus, Coffea Cruda, Ferrum Phosphoricum, Kali Phosphoricum, Magnesia Carbonica, Melatonin, Natrum Muriaticum, Nux Vomica, Pulsatilla (Pratensis)
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2019-03-25
- Marketing end
- 2020-05-08
- Substance
- OYSTER SHELL CALCIUM CARBONATE, CRUDE; MATRICARIA CHAMOMILLA; ANAMIRTA COCCULUS SEED; ARABICA COFFEE BEAN; FERROSOFERRIC PHOSPHATE; DIBASIC POTASSIUM PHOSPHATE; MAGNESIUM CARBONATE; MELATONIN; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; ANEMONE PRATENSIS
- Active strength
- 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record