- Product NDC
- 57955-5149
- 11-digit product format
- 579555149
- Labeler code
- 57955
- Product ID
- 57955-5149_824033ce-024d-4287-9b69-fdc94a21e9f1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum napellus, Arsenicum album, Baryta carbonica, Cantharis, Gelsemium sempervirens, Graphites, Hydrastis canadensis, Kali iodatum, Lachesis mutus, Lycopodium clavatum, Mercurius vivus, Natrum muriaticum, Nux vomica, Phosphorus, Phytolacca decandra, Pulsatilla, Rhus toxicodendron, Sepia, Silicea and Sulphur
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- King Bio Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-03-21
- Marketing end
- 0000-00-00
- Substance
- ACONITUM NAPELLUS; ARSENIC TRIOXIDE; BARIUM CARBONATE; BRYONIA ALBA ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; LYTTA VESICATORIA; GELSEMIUM SEMPERVIRENS ROOT; GRAPHITE; GOLDENSEAL; POTASSIUM IODIDE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; MERCURY; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; PHYTOLACCA AMERICANA ROOT; PULSATILLA VULGARIS; TOXICODENDRON PUBESCENS LEAF; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SULFUR; PHOSPHORUS
- Active strength
- 30 [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; [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