- Product NDC
- 54705-000
- 11-digit product format
- 547050000
- Labeler code
- 54705
- Product ID
- 54705-000_3a60bfad-ad5f-4284-a75e-d170e0990e60
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allium cepa, Ambrosia artemisiaefolia, Apis mellifica, Chamomilla, Eucalyptol, Eucalyptus globulus, Euphrasia officinalis, Galphimia glauca, Histaminum hydrochloricum, Natrum muriaticum, Nux vomica, Quercus robur, Silicea, Wyethia helenioides
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Flutrends International Corporation
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-10-28
- Marketing end
- 0000-00-00
- Substance
- ONION; AMBROSIA ARTEMISIIFOLIA; APIS MELLIFERA; MATRICARIA RECUTITA; EUCALYPTOL; EUCALYPTUS GLOBULUS LEAF; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; QUERCUS ROBUR TWIG BARK; SILICON DIOXIDE; WYETHIA HELENIOIDES ROOT
- Active strength
- 10 [hp_X]/28mL; [hp_X]/28mL; [hp_X]/28mL; [hp_X]/28mL; [hp_X]/28mL; [hp_X]/28mL; [hp_X]/28mL; [hp_X]/28mL; [hp_X]/28mL; [hp_X]/28mL; [hp_X]/28mL; [hp_X]/28mL; [hp_X]/28mL; [hp_X]/28mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record