- Product NDC
- 57955-0420
- 11-digit product format
- 579550420
- Labeler code
- 57955
- Product ID
- 57955-0420_22b9f571-1f43-40b9-b809-0a0391b3b86a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Adrenalinum, Argentum iodatum, Cadmium sulphuricum, Capsicum Annuum, Fucus vesiculosus, Iodium, Kali iodatum, Ledum palustre, Lycopodium clavatum, Phosphoricum acidum, Phosphorus, Pulsatilla, Radium bromatum Strontium carbonicum, Thyroidinum, Uranium nitricum, X-ray
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- King Bio Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-04-17
- Marketing end
- 0000-00-00
- Substance
- EPINEPHRINE; SILVER IODIDE; CADMIUM SULFATE; CAPSICUM; FUCUS VESICULOSUS; IODINE; POTASSIUM IODIDE; LEDUM PALUSTRE TWIG; LYCOPODIUM CLAVATUM SPORE; PHOSPHORIC ACID; PHOSPHORUS; PULSATILLA VULGARIS; RADIUM BROMIDE; STRONTIUM CARBONATE; THYROID, UNSPECIFIED; URANYL NITRATE HEXAHYDRATE; ALCOHOL, X-RAY EXPOSED (1000 RAD)
- 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
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record