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


Net Remedies
Human Prescription Drug
NDC 61626-0110
Er 911 also known as 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 is a human prescription drug labeled by 'Net Remedies'. National Drug Code (NDC) number for Er 911 is 61626-0110. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Er 911 drug includes 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 and more. The currest status of Er 911 drug is Active.

Drug Information:

Drug NDC: 61626-0110
The 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.
Proprietary Name: Er 911
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Prescription Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
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
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Net Remedies
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name: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 - 12 [hp_X]/59.1mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date: 04 Dec, 2018
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 13 Jan, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Net Remedies
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
NUI:N0000185021
N0000175629
N0000184306
N0000185001
M0000728
M0002274
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:U0NQ8555JD
7S82P3R43Z
O80TY208ZW
S7V92P67HO
WQZ3G9PF0H
2HU33I03UY
T7J046YI2B
18E7415PXQ
396421SP9F
M9VVZ08EKQ
91GQH8I5F7
46G3W789Q3
3POA0Q644U
XK4IUX8MNB
AJU5O1A5ZV
G0R4UBI2ZZ
9NS3M2Y78S
CLF5YFS11O
27YLU75U4W
0KD7R09EAS
1NM3M2487K
70FD1KFU70
6IO182RP7A
QNS6W5US1Z
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:Standardized Insect Venom Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:Increased Histamine Release [PE]
Cell-mediated Immunity [PE]
Increased IgG Production [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:Allergens [CS]
Bee Venoms [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:Allergens [CS]
Bee Venoms [CS]
Cell-mediated Immunity [PE]
Increased Histamine Release [PE]
Increased IgG Production [PE]
Standardized Insect Venom Allergenic Extract [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
61626-0110-459.1 mL in 1 BOTTLE (61626-0110-4)04 Dec, 2018N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Purpose:

Indications for use: for the temporary relief of emotional, mental, or physical trauma, high pressure or stressful situations • symptomatic relief of nervous tension, stress, dread and fever. temporary relief of cold and flu-like symptoms. overexertion • strains • tearfulness • fearfulness • oversensitivity • minor nerve pain and burning • quieting effect on nervous system.**

Product Elements:

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 citric acid monohydrate potassium sorbate water aconitum napellus aconitum napellus apis mellifera apis mellifera arnica montana arnica montana arsenic trioxide arsenic cation (3+) atropa belladonna atropa belladonna bellis perennis bellis perennis bryonia alba root bryonia alba root calendula officinalis flowering top calendula officinalis flowering top matricaria chamomilla matricaria chamomilla helianthemum canadense helianthemum canadense clematis recta flowering top clematis recta flowering top ferrosoferric phosphate ferrosoferric phosphate histamine dihydrochloride histamine hypericum perforatum hypericum perforatum strychnos ignatii seed strychnos ignatii seed impatiens glandulifera flower impatiens glandulifera flower ornithogalum umbellatum ornithogalum umbellatum passiflora incarnata flowering top passiflora incarnata flowering top phosphorus phosphorus prunus cerasifera flower prunus cerasifera flower toxicodendron pubescens leaf toxicodendron pubescens leaf sulfur sulfur comfrey root comfrey root veratrum album root veratrum album root

Indications and Usage:

​indications for use: for the temporary relief of emotional, mental, or physical trauma, high pressure or stressful situations • symptomatic relief of nervous tension, stress, dread and fever. temporary relief of cold and flu-like symptoms. overexertion ​ ​• strains • tearfulness • fearfulness • oversensitivity • minor nerve pain and burning ​• quieting effect on nervous system.**

Warnings:

​warnings: • ​if sumptoms persist or worsen ​, seek advice of licensed health care practitioner. • ​if pregnant or nursing ​, take on advice of licensed health care practitioner. ​ ​• ​keep this and all medication out of reach of children. • keep this and all medication out of reach of children.

Dosage and Administration:

​directions: ​spray 9-12 pumps (approximately 1/2 tsp.) directly in mouth 3 times a day or as direced by licensed health care practitioner. when appropriate, also spray externally on complaint area 3 times daily.

Package Label Principal Display Panel:

​net remedies #9 er 911 homeopathic preparation ​professional formula ​naturally no side effects er 911 bottle label indications for use: for the temporary relief of emotional, mental, or physical trauma, high pressure or stressful situations • symptomatic relief of nervous tension, stress, dread and fever. temporary relief of cold and flu-like symptoms. overexertion • strains • tearfulness • fearfulness • oversensitivity • minor nerve pain and burning • quieting effect on nervous system.**

Further Questions:

​www.netmindbody.com made in the usa


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.