- Product NDC
- 35378-0010
- 11-digit product format
- 353780010
- Labeler code
- 35378
- Product ID
- 35378-0010_7cee29cf-2094-93b8-4113-2bc3fccf739b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum nap., Antimon. tart., Arg. nit., Arnica, Bryona, Chamomilla, Chelidonium majus, Cimicifuga, Eupatorium perf., Hypericum, Nux vom., Rhus toxicodendron, Ruta, Sarcolacticum ac., Stramonium, Strychnium, Chamomilla, Phytolacca, Ruta, Symphytum
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Georgetown Health, LLC DBA EssentiaLife
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-07-01
- Marketing end
- 0000-00-00
- Substance
- ACONITUM NAPELLUS; ANTIMONY POTASSIUM TARTRATE; SILVER NITRATE; ARNICA MONTANA; BRYONIA ALBA ROOT; MATRICARIA RECUTITA; CHELIDONIUM MAJUS; BLACK COHOSH; EUPATORIUM PERFOLIATUM FLOWERING TOP; HYPERICUM PERFORATUM; STRYCHNOS NUX-VOMICA SEED; TOXICODENDRON PUBESCENS LEAF; RUTA GRAVEOLENS FLOWERING TOP; LACTIC ACID, L-; DATURA STRAMONIUM; STRYCHNINE; MATRICARIA RECUTITA; PHYTOLACCA AMERICANA ROOT; RUTA GRAVEOLENS FLOWERING TOP; COMFREY ROOT
- Active strength
- 15 [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record