- Product NDC
- 57955-2541
- 11-digit product format
- 579552541
- Labeler code
- 57955
- Product ID
- 57955-2541_f01056f3-5535-420d-a2cb-5e7c96823eca
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ceratostigma willmottianum, flos, Chamomilla, Chelidonium majus, Graphites, Ilex aquifolium, flos, Kali bromatum, Lachesis mutus, Malus pumila, flos, Millefolium, Pinus sylvestris, flos, Psorinum, Stramonium, Sulphur, Veratrum album
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- King Bio Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-08-10
- Marketing end
- 0000-00-00
- Substance
- CERATOSTIGMA WILLMOTTIANUM FLOWER; MATRICARIA RECUTITA; CHELIDONIUM MAJUS; GRAPHITE; ILEX AQUIFOLIUM FLOWERING TOP; POTASSIUM BROMIDE; LACHESIS MUTA VENOM; MALUS DOMESTICA FLOWER; ACHILLEA MILLEFOLIUM; PINUS SYLVESTRIS FLOWERING TOP; SCABIES LESION LYSATE (HUMAN); DATURA STRAMONIUM; SULFUR; VERATRUM ALBUM ROOT
- 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
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record