- Product NDC
- 68703-111
- 11-digit product format
- 687030111
- Labeler code
- 68703
- Product ID
- 68703-111_8adb5cf3-9e65-4f3c-9c65-32e93fc806fc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Adenosinum cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Alfalfa, Allium cepa, Bellis perennis, Conium maculatum, Cortisone aceticum, Equisetum hyemale, Euphrasia officinalis, Fogopyrum esculentum, Galphimia glauca, Histaminum hydrochloricum, kali muriaticum, Millefolium, Mucosa nasalis suis, Natrum muriaticum, Prunus spinosa, RNA, Sabadilla, Solidago virgaurea
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Native Remedies, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-07-01
- Marketing end
- 0000-00-00
- Substance
- ADENOSINE CYCLIC PHOSPHATE; EPINEPHRINE; CORTICOTROPIN; ALFALFA; ONION; BELLIS PERENNIS; CONIUM MACULATUM FLOWERING TOP; CORTISONE ACETATE; EQUISETUM HYEMALE; EUPHRASIA STRICTA; FAGOPYRUM ESCULENTUM; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; POTASSIUM CHLORIDE; ACHILLEA MILLEFOLIUM; SUS SCROFA NASAL MUCOSA; SODIUM CHLORIDE; PRUNUS SPINOSA FLOWER BUD; SACCHAROMYCES CEREVISIAE RNA; SCHOENOCAULON OFFICINALE SEED; SOLIDAGO VIRGAUREA FLOWERING TOP
- Active strength
- 12 h/59mL; h/59mL; h/59mL; h/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; h/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