- Product NDC
- 57955-4020
- 11-digit product format
- 579554020
- Labeler code
- 57955
- Product ID
- 57955-4020_bfc666ea-c9f7-472e-8aee-0c79615e7871
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aloe socotrina, Carbo vegetabilis, Chamomilla, Cinchona officinalis, Collinsonia canadensis, Colocynthis, Croton tiglium, Gelsemium sempervirens, Gratiola officinalis, Nux vomica,Phosphoricum acidum, Podophyllum peltatum and Veratrum album
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- King Bio Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-02-13
- Marketing end
- 0000-00-00
- Substance
- ALOE; ACTIVATED CHARCOAL; MATRICARIA RECUTITA; CINCHONA OFFICINALIS BARK; COLLINSONIA CANADENSIS ROOT; CITRULLUS COLOCYNTHIS FRUIT PULP; CROTON TIGLIUM SEED; GELSEMIUM SEMPERVIRENS ROOT; GRATIOLA OFFICINALIS; STRYCHNOS NUX-VOMICA SEED; PHOSPHORIC ACID; PODOPHYLLUM; VERATRUM ALBUM ROOT
- Active strength
- 10 [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; mL/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record