- Product NDC
- 66579-0079
- 11-digit product format
- 665790079
- Labeler code
- 66579
- Product ID
- 66579-0079_e915d6b6-3b00-430c-82e2-18b1f187c9d6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum napellus, Allium cepa, Ambrosia artemisiaefolia, Apis mellifica, arsenicum album, Belladonna, Cactus grandiflorus, Dulcamara, Euphrasia officinalis, Gelsemium sempervirens, Graphites, Hamamelis virginiana, Hepar sulphuris calcareum, Kali iodatum, Mercurius vivus, Natrum muriaticum, Pulsatilla, Rhus toxicodendron, Ruta graveolens, Sabadilla, Sulphur, Thuja occidentalis, Zincum metallicum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- New Sun Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-10-20
- Marketing end
- 0000-00-00
- Substance
- ACONITUM NAPELLUS; ONION; AMBROSIA ARTEMISIIFOLIA; APIS MELLIFERA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; SELENICEREUS GRANDIFLORUS STEM; SOLANUM DULCAMARA TOP; EUPHRASIA STRICTA; GELSEMIUM SEMPERVIRENS ROOT; GRAPHITE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; CALCIUM SULFIDE; POTASSIUM IODIDE; MERCURY; SODIUM CHLORIDE; PULSATILLA VULGARIS; TOXICODENDRON PUBESCENS LEAF; RUTA GRAVEOLENS FLOWERING TOP; SCHOENOCAULON OFFICINALE SEED; SULFUR; THUJA OCCIDENTALIS LEAFY TWIG; ZINC
- Active strength
- 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record