- Product NDC
- 48951-1358
- 11-digit product format
- 489511358
- Labeler code
- 48951
- Product ID
- 48951-1358_eac58c77-dbf6-c9ee-e053-2a95a90a70e1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Argentum Veratrum
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Uriel Pharmacy, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- APIS MELLIFERA; BOS TAURUS PARATHYROID GLAND; CUPRIC SULFATE; GOLD; MAGNESIUM SULFATE, UNSPECIFIED; PHOSPHORUS; ROYAL JELLY; SILVER; SUGARCANE; SUS SCROFA PANCREAS; TARAXACUM PALUSTRE ROOT; URTICA DIOICA; VERATRUM ALBUM ROOT
- Active strength
- 5 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- Pharmacologic classes
- Allergens [CS], Allergens [CS], Bee Venoms [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Standardized Chemical Allergen [EPC], Standardized Insect Venom Allergenic Extract [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record