- Product NDC
- 57955-1803
- 11-digit product format
- 579551803
- Labeler code
- 57955
- Product ID
- 57955-1803_2d6a56c6-3d77-478d-a83e-cad3b91adfdd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum napellus, Adrenalinum, Ammonium carbonicum, Antimonium tartaricum, Aralia racemosa, Bromium, Chlorinum, Eriodictyon californicum, Eucalyptus globulus, Grindelia, Lobelia inflata, Natrum sulphuricum, Phosphorus, Quebracho, Trifolium pratense
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- King Bio Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-08-06
- Marketing end
- 0000-00-00
- Substance
- ACONITUM NAPELLUS; EPINEPHRINE; AMMONIUM CARBONATE; ANTIMONY POTASSIUM TARTRATE; ARALIA RACEMOSA ROOT; BROMINE; CHLORINE; ERIODICTYON CALIFORNICUM LEAF; EUCALYPTUS GLOBULUS LEAF; GRINDELIA HIRSUTULA FLOWERING TOP; LOBELIA INFLATA; SODIUM SULFATE; PHOSPHORUS; ASPIDOSPERMA QUEBRACHO-BLANCO BARK; TRIFOLIUM PRATENSE FLOWER
- 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
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record