Earth

Aur Met, Arg Nit, Causticum, Cinchona, Condurango, Ceanothus, Euphrasia, Fucus, Gallicum Ac, Iris Vers, Net Carb, Nitricum Ac, Phosphorus.

Net Remedies
Human Otc Drug
NDC 61626-0102

Earth also known as Aur Met, Arg Nit, Causticum, Cinchona, Condurango, Ceanothus, Euphrasia, Fucus, Gallicum Ac, Iris Vers, Net Carb, Nitricum Ac, Phosphorus. is a human otc drug labeled by 'Net Remedies'. National Drug Code (NDC) number for Earth is 61626-0102. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Earth drug includes Causticum - 12 [hp_X]/59mL Ceanothus Americanus Leaf - 12 [hp_X]/59mL Cinchona Officinalis Bark - 12 [hp_X]/59mL Euphrasia Stricta - 12 [hp_X]/59mL Fucus Vesiculosus - 12 [hp_X]/59mL Gallic Acid Monohydrate - 12 [hp_X]/59mL Gold - 12 [hp_X]/59mL Iris Versicolor Root - 12 [hp_X]/59mL Marsdenia Condurango Bark - 12 [hp_X]/59mL Nitric Acid - 12 [hp_X]/59mL and more. The currest status of Earth drug is Active.

Drug Information:

Drug NDC:	61626-0102
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:	Earth
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc 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:	Aur Met, Arg Nit, Causticum, Cinchona, Condurango, Ceanothus, Euphrasia, Fucus, Gallicum Ac, Iris Vers, Net Carb, Nitricum Ac, Phosphorus.
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:	CAUSTICUM - 12 [hp_X]/59mL CEANOTHUS AMERICANUS LEAF - 12 [hp_X]/59mL CINCHONA OFFICINALIS BARK - 12 [hp_X]/59mL EUPHRASIA STRICTA - 12 [hp_X]/59mL FUCUS VESICULOSUS - 12 [hp_X]/59mL GALLIC ACID MONOHYDRATE - 12 [hp_X]/59mL GOLD - 12 [hp_X]/59mL IRIS VERSICOLOR ROOT - 12 [hp_X]/59mL MARSDENIA CONDURANGO BARK - 12 [hp_X]/59mL NITRIC ACID - 12 [hp_X]/59mL Load more... PHOSPHORUS - 12 [hp_X]/59mL SILVER NITRATE - 12 [hp_X]/59mL SODIUM CARBONATE - 12 [hp_X]/59mL
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:	10 Jun, 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:	N0000185508 N0000175629 N0000184306 M0000728
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	DD5FO1WKFU 25B1Y14T8N S003A158SB C9642I91WL 535G2ABX9M 48339473OT 79Y1949PYO X43D4L3DQC R23QIR6YBA 411VRN1TV4 Load more... 27YLU75U4W 95IT3W8JZE 45P3261C7T
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 Chemical Allergen [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]
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]
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] Cell-mediated Immunity [PE] Increased Histamine Release [PE] Standardized Chemical Allergen [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
61626-0102-4	59 mL in 1 BOTTLE (61626-0102-4)	04 Dec, 2018	N/A	No
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.

Other medicines with the same generic name

Earth

Aur Met & more..

Liquid
NET Remedies
NDC: 61626-0102

Purpose:

For the temporary relief of the neuro-emotional (automatic nervous system - non psychiatric) disorders of oversympathy, low self esteem and related emotions. sensory, spinal and extremity disorders. relief of symptoms of colds, sinus problems. digestive, mouth saliva, taste disorders. weak spine and lower extremity disorders.**

Product Elements:

Earth aur met, arg nit, causticum, cinchona, condurango, ceanothus, euphrasia, fucus, gallicum ac, iris vers, net carb, nitricum ac, phosphorus. citric acid monohydrate potassium sorbate water gold gold silver nitrate silver cation causticum causticum cinchona officinalis bark cinchona officinalis bark marsdenia condurango bark marsdenia condurango bark ceanothus americanus leaf ceanothus americanus leaf euphrasia stricta euphrasia stricta fucus vesiculosus fucus vesiculosus gallic acid monohydrate gallic acid iris versicolor root iris versicolor root sodium carbonate carbonate ion nitric acid nitric acid phosphorus phosphorus

Indications and Usage:

âindications for use: for the temporary relief of the neuro-emotional (automatic nervous system - non psychiatric) disorders of oversympathy, low self esteem and related emotions. sensory, spinal and extremity disorders. relief of symptoms of colds, sinus problems. digestive, mouth saliva, taste disorders. weak spine and lower extremity disorders.**â

Warnings:

âwarnings: â¢ âif symptoms persist or worsen, âseek advice of licensed health care practicioner. â¢ âif pregnant or nursing â, take only on advice of licensed health care practicioner. â¢ âkeep this and all medication out of reach of children. â¢ keep this and all medication out of reach of children.

Dosage and Administration:

â âdirections: âspray 9-12 pumps (approximately 1/2 tsp.) directly in mouth 3 times a day or as directed by a licensed health care practicioner. when appropriate, also spray externalyl on complaint area 3 times daily.

Package Label Principal Display Panel:

ânet remedies #1 earth homeopathic preparation spleen & stomach meridans professional formula ânaturally no side effects â â2 fl oz (59 ml) earth 2 fl oz bottle label for the temporary relief of the neuro-emotional (automatic nervous system - non psychiatric) disorders of oversympathy, low self esteem and related emotions. sensory, spinal and extremity disorders. relief of symptoms of colds, sinus problems. digestive, mouth saliva, taste disorders. weak spine and lower extremity disorders.**

Further Questions:

âwww.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.