- Product NDC
- 57955-2030
- 11-digit product format
- 579552030
- Labeler code
- 57955
- Product ID
- 57955-2030_7715ac5b-1e4c-4ed1-a192-521a165dbead
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aloe socotrina, Ambra grisea, Ammonium muriaticum, Antimonium crudum, Aurum metallicum, Borago officinalis, Cichorium intybus, flos, Cimicifuga racemosa, Eriodictyon californicum, Ignatia amara, Ilex aquifolium, flos, Iodium, Natrum muriaticum, Phosphoricum acidum, Rosa damascena, Stannum metallicum, Tilia europaea
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- King Bio Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-08-12
- Marketing end
- 0000-00-00
- Substance
- ALOE; AMBERGRIS; AMMONIUM CHLORIDE; ANTIMONY TRISULFIDE; GOLD; BORAGE; CICHORIUM INTYBUS FLOWER; BLACK COHOSH; ERIODICTYON CALIFORNICUM LEAF; STRYCHNOS IGNATII SEED; ILEX AQUIFOLIUM FLOWERING TOP; IODINE; SODIUM CHLORIDE; PHOSPHORIC ACID; ROSA DAMASCENA FLOWERING TOP; TIN; TILIA X EUROPAEA 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; [hp_X]/59mL; [hp_X]/59mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record