- Product NDC
- 43772-0038
- 11-digit product format
- 437720038
- Labeler code
- 43772
- Product ID
- 43772-0038_4b58c4de-2677-4791-ac10-a3119fe7923b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Echinacea (Angustifolia), Hydrastis Canadensis, Lycopodium Clavatum, Nasturtium Aquaticum, Taraxacum Officinale, Trifolium Pratense, Rhus Tox, Arnica Montana, Glandula Suprarenalis Suis, Medulla Ossis Suis, Thymus (Suis), Oxalicum Acidum, Magnesia Phosphorica, Latrodectus Mactans, Borrelia Burgdorferi Nosode, Encephalitis Nosode, Meningococcus Nosode, Hepatitis B Nosode
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Synergy Formulas, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-07-15
- Marketing end
- 0000-00-00
- Substance
- ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; LYCOPODIUM CLAVATUM SPORE; NASTURTIUM OFFICINALE; TARAXACUM OFFICINALE; TRIFOLIUM PRATENSE FLOWER; TOXICODENDRON PUBESCENS LEAF; ARNICA MONTANA; SUS SCROFA ADRENAL GLAND; SUS SCROFA BONE MARROW; SUS SCROFA THYMUS; OXALIC ACID; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; LATRODECTUS MACTANS; BORRELIA BURGDORFERI; JAPANESE ENCEPHALITIS VIRUS; NEISSERIA MENINGITIDIS; HEPATITIS B VIRUS
- 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; [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