- Product NDC
- 66579-0026
- 11-digit product format
- 665790026
- Labeler code
- 66579
- Product ID
- 66579-0026_da840a58-8724-4b2c-b0f6-2d3c698fd793
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Apis mellifica, Baptisia tinctoria, Colocythis, Hepar sulphuris calcareum, Histaminum hydrochloricum, Hydrastis canadensis, Ignatia amara, Kali bichromicum, Lemna minor, Mercurius vivus, Pulsatilla, Rhus toxicodendron, Sabadilla, Thuja occidentalis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- New Sun Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-07-17
- Marketing end
- 0000-00-00
- Substance
- APIS MELLIFERA; BAPTISIA TINCTORIA ROOT; CITRULLUS COLOCYNTHIS FRUIT PULP; CALCIUM SULFIDE; HISTAMINE DIHYDROCHLORIDE; GOLDENSEAL; STRYCHNOS IGNATII SEED; POTASSIUM DICHROMATE; LEMNA MINOR; MERCURY; PULSATILLA VULGARIS; TOXICODENDRON PUBESCENS LEAF; SCHOENOCAULON OFFICINALE SEED; THUJA OCCIDENTALIS LEAFY TWIG
- 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
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record