- Product NDC
- 57520-0099
- 11-digit product format
- 575200099
- Labeler code
- 57520
- Product ID
- 57520-0099_3715c74f-6dab-456a-bd34-efdd7c629615
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Echinacea angustifolia, Hydrastis canadensis, Lomatium, Nasturtium aquaticum, Tabebuia impetiginosa, Iodium, Adrenalinum, Argentum metallicum, Thymus, Thyroidinum, Phosphoricum acidum, Candida albicans, Lycopodium clavatum, Pulsatilla, Sepia
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Apotheca Company
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2010-02-17
- Marketing end
- 0000-00-00
- Substance
- ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; LOMATIUM DISSECTUM ROOT; TABEBUIA IMPETIGINOSA BARK; IODINE; EPINEPHRINE; SILVER; SUS SCROFA THYMUS; THYROID, UNSPECIFIED; PHOSPHORIC ACID; CANDIDA ALBICANS; LYCOPODIUM CLAVATUM SPORE; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; RORIPPA NASTURTIUM-AQUATICUM
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record