- Product NDC
- 43742-1665
- 11-digit product format
- 437421665
- Labeler code
- 43742
- Product ID
- 43742-1665_446da5cc-e452-4416-a9c4-0788ddc3106b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Arnica Montana, Cinnamomum, Dulcamara, Funiculus Umbilicalis Suis, Nadidum, Natrum Oxalaceticum, Pantothenic Acid, Placenta Totalis Suis, Sanguinaria Canadensis, Sulphur, Piper Nigrum, Alpha-Lipoicum Acidum, Cartilago Suis, Rhus Tox, Silicea, Symphytum Officinale, Thuja Occidentalis, Apiolum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-06-15
- Marketing end
- 2029-05-20
- Substance
- ALPHA LIPOIC ACID; APIOLE (PARSLEY); ARNICA MONTANA WHOLE; CINNAMON; COMFREY ROOT; GREEN PEPPERCORN; NADIDE; PANTOTHENIC ACID; SANGUINARIA CANADENSIS ROOT; SILICON DIOXIDE; SODIUM DIETHYL OXALACETATE; SOLANUM DULCAMARA TOP; SULFUR; SUS SCROFA CARTILAGE; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS LEAF
- Active strength
- 8; 16; 3; 6; 8; 6; 6; 6; 6; 8; 6; 6; 6; 8; 6; 6; 12; 8 [hp_X]/mL; [hp_C]/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
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC]
- NDC exclude flag
- No
- Current FDA listing
- Yes