61626-0110 NDC - ER 911 (ACONITUM NAP, APIS MEL, ARNICA, ARSENICUM ALB, BELLADONNA, BELLIS, BRYONIA, CALENDULA, CHAMOMILLA, CISTUS CANADENSIS, CLEMATIS ERECTA, FERRUM PHOS, HISTAMINUM, HYPERICUM, IGNATIA, IMPATIENS GLAN FLOS, ORNITHOGALUM, PASSIFLORA, PHOSPHORUS, PRUNUS CERASIFERA, RHUS TOX, SULPHUR, SYMPHYTUM, VERTARUM ALB)

Drug Information

  • Product NDC: 61626-0110
  • Proprietary Name: ER 911
  • Non Proprietary Name: Aconitum nap, Apis mel, Arnica, Arsenicum alb, Belladonna, Bellis, Bryonia, Calendula, Chamomilla, Cistus canadensis, Clematis erecta, Ferrum phos, Histaminum, Hypericum, Ignatia, Impatiens glan flos, Ornithogalum, Passiflora, Phosphorus, Prunus cerasifera, Rhus tox, Sulphur, Symphytum, Vertarum alb
  • Active Ingredient(s): 12 [hp_X]/59.1mL ACONITUM NAPELLUS; 12 [hp_X]/59.1mL APIS MELLIFERA; 12 [hp_X]/59.1mL ARNICA MONTANA; 12 [hp_X]/59.1mL ARSENIC TRIOXIDE; 12 [hp_X]/59.1mL ATROPA BELLADONNA; 12 [hp_X]/59.1mL BELLIS PERENNIS; 12 [hp_X]/59.1mL BRYONIA ALBA ROOT; 12 [hp_X]/59.1mL CALENDULA OFFICINALIS FLOWERING TOP; 12 [hp_X]/59.1mL CLEMATIS RECTA FLOWERING TOP; 12 [hp_X]/59.1mL COMFREY ROOT; 12 [hp_X]/59.1mL FERROSOFERRIC PHOSPHATE; 12 [hp_X]/59.1mL HELIANTHEMUM CANADENSE; 12 [hp_X]/59.1mL HISTAMINE DIHYDROCHLORIDE; 12 [hp_X]/59.1mL HYPERICUM PERFORATUM; 12 [hp_X]/59.1mL IMPATIENS GLANDULIFERA FLOWER; 12 [hp_X]/59.1mL MATRICARIA CHAMOMILLA; 12 [hp_X]/59.1mL ORNITHOGALUM UMBELLATUM; 12 [hp_X]/59.1mL PASSIFLORA INCARNATA FLOWERING TOP; 12 [hp_X]/59.1mL PHOSPHORUS; 12 [hp_X]/59.1mL PRUNUS CERASIFERA FLOWER; 12 [hp_X]/59.1mL STRYCHNOS IGNATII SEED; 12 [hp_X]/59.1mL SULFUR; 12 [hp_X]/59.1mL TOXICODENDRON PUBESCENS LEAF; 12 [hp_X]/59.1mL VERATRUM ALBUM ROOT
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Standardized Insect Venom Allergenic Extract [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Net Remedies
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:12/4/2018

Package Information

No. Package Code Package Description Billing Unit
161626-0110-459.1 mL in 1 BOTTLE (61626-0110-4)

NDC Record

Field Name Field Value Definition
PRODUCT NDC61626-0110The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEER 911The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAconitum nap, Apis mel, Arnica, Arsenicum alb, Belladonna, Bellis, Bryonia, Calendula, Chamomilla, Cistus canadensis, Clematis erecta, Ferrum phos, Histaminum, Hypericum, Ignatia, Impatiens glan flos, Ornithogalum, Passiflora, Phosphorus, Prunus cerasifera, Rhus tox, Sulphur, Symphytum, Vertarum albThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE12/4/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMENet RemediesName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACONITUM NAPELLUS; APIS MELLIFERA; ARNICA MONTANA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BELLIS PERENNIS; BRYONIA ALBA ROOT; CALENDULA OFFICINALIS FLOWERING TOP; CLEMATIS RECTA FLOWERING TOP; COMFREY ROOT; FERROSOFERRIC PHOSPHATE; HELIANTHEMUM CANADENSE; HISTAMINE DIHYDROCHLORIDE; HYPERICUM PERFORATUM; IMPATIENS GLANDULIFERA FLOWER; MATRICARIA CHAMOMILLA; ORNITHOGALUM UMBELLATUM; PASSIFLORA INCARNATA FLOWERING TOP; PHOSPHORUS; PRUNUS CERASIFERA FLOWER; STRYCHNOS IGNATII SEED; SULFUR; TOXICODENDRON PUBESCENS LEAF; VERATRUM ALBUM ROOTAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12 
ACTIVE INGRED UNIT[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL 
PHARM CLASSESAllergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC] 

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This page was last updated on: 5/26/2025

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