- Product NDC
- 57955-5319
- 11-digit product format
- 579555319
- Labeler code
- 57955
- Product ID
- 57955-5319_00674758-a35a-45c4-98b5-46d5e55758e9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ammonium carbonicum, Asafoetida, Baptisia tinctoria, Carbo vegetabilis, Carbolicum acidum, Graphites, Kreosotum, Mercurius corrosivus, Oleander, Phosphorus, Rhus toxicodendron and Zincum metallicum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- King Bio Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-02-27
- Marketing end
- 0000-00-00
- Substance
- AMMONIUM CARBONATE; ASAFETIDA; BAPTISIA TINCTORIA ROOT; ACTIVATED CHARCOAL; PHENOL; GRAPHITE; WOOD CREOSOTE; MERCURIC CHLORIDE; NERIUM OLEANDER LEAF; PHOSPHORUS; TOXICODENDRON PUBESCENS LEAF; ZINC
- 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
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record