- Product NDC
- 57955-0753
- 11-digit product format
- 579550753
- Labeler code
- 57955
- Product ID
- 57955-0753_a9ef424c-d84c-b5bc-e053-2995a90aa6f4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Adenosinum cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Agraphis nutans, Allium cepa, Collinsonia canadensis, Cortisone aceticum, Euphrasia officinalis, Galphimia glauca, Histaminum hydrochloricum, Kali muriaticum, Mucosa nasalis suis, Natrum muriaticum, RNA, Rumex crispus, Sabadilla, Salvia officinalis, Tanacetum vulgare, Trifolium pratense, Vinca minor
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- King Bio Inc,
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-02-21
- Marketing end
- 0000-00-00
- Substance
- ADENOSINE CYCLIC PHOSPHATE; EPINEPHRINE; CORTICOTROPIN; HYACINTHOIDES NON-SCRIPTA; ONION; COLLINSONIA CANADENSIS ROOT; CORTISONE ACETATE; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; POTASSIUM CHLORIDE; SUS SCROFA NASAL MUCOSA; SODIUM CHLORIDE; SACCHAROMYCES CEREVISIAE RNA; RUMEX CRISPUS ROOT; SCHOENOCAULON OFFICINALE SEED; SAGE; TANACETUM VULGARE TOP; TRIFOLIUM PRATENSE FLOWER; VINCA MINOR
- Active strength
- 12 [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
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record