- Product NDC
- 64578-0055
- 11-digit product format
- 645780055
- Labeler code
- 64578
- Product ID
- 64578-0055_6a481836-73ff-4591-ab8a-3cce1630429c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arsenicum Album, Belladonna, Calcarea Carbonica, Ceanothus Americanus, Chelidonium Majus, Cuprum Sulphuricum, Fumaricum Acidum, Galium Aparine, Glandula Suprarenalis Suis, Hepar Suis, Kali Iodatum, Lycopodium Clavatum, Pancreas Suis, Petroleum, Phosphoricum Acidum, Phosphorus, Phytolacca Decandra, Sarsaparilla (Smilax Regelii), Silicea, Sulphur, Thyroidinum (Bovine), Trifolium Pratense, Xanthoxylum Fraxineum, Zincum Phosphoratum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energetix Corp
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-11-17
- Marketing end
- 0000-00-00
- Substance
- ARSENIC TRIOXIDE; ATROPA BELLADONNA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CEANOTHUS AMERICANUS LEAF; CHELIDONIUM MAJUS; CUPRIC SULFATE; FUMARIC ACID; GALIUM APARINE; SUS SCROFA ADRENAL GLAND; PORK LIVER; POTASSIUM IODIDE; LYCOPODIUM CLAVATUM SPORE; SUS SCROFA PANCREAS; KEROSENE; PHOSPHORIC ACID; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; SMILAX REGELII ROOT; SILICON DIOXIDE; SULFUR; THYROID, BOVINE; TRIFOLIUM PRATENSE FLOWER; ZANTHOXYLUM AMERICANUM BARK; ZINC PHOSPHIDE
- Active strength
- 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record