- Product NDC
- 66579-0090
- 11-digit product format
- 665790090
- Labeler code
- 66579
- Product ID
- 66579-0090_18089f3e-d601-4140-a539-49256ab77a25
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arsenicum album, Baptisia tinctoria, Bryonia, Dulcamara, Echinacea, Echinacea purpurea, Eupatorium purpureum, Ferrum phosphoricum, Gelsemium sempervirens, Kali muriaticum, Phosphorus, Pulsatilla, Sulphur, Zincum aceticum, Zincum carbonicum, Zincum metallicum, Zincum muriaticum, Zincum oxydatum, Zincum picricum, Zincum valerianicum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- New Sun Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-08-20
- Marketing end
- 0000-00-00
- Substance
- ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BRYONIA ALBA ROOT; SOLANUM DULCAMARA TOP; ECHINACEA, UNSPECIFIED; ECHINACEA PURPUREA; FERROSOFERRIC PHOSPHATE; GELSEMIUM SEMPERVIRENS ROOT; POTASSIUM CHLORIDE; PHOSPHORUS; PULSATILLA VULGARIS; SULFUR; ZINC ACETATE ANHYDROUS; ZINC CARBONATE; ZINC; ZINC CHLORIDE; ZINC OXIDE; ZINC PICRATE NONAHYDRATE; ZINC VALERATE DIHYDRATE
- 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; [hp_X]/59mL; [hp_X]/59mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record