Emf

Argentum Nitricum, Arnica Montana, Baptisia Tinctoria, Cinchona Officinalis, Galium Aparine, Hepar Suis, Natrum Carbonicum, Panax Ginseng, Phosphoricum Acidum, Phosphorus, Rhododendron Chrysanthum, Strontium Carbonicum, Sulphur Iodatum, Thuja Occidentalis, X-ray

Liddell Laboratories, Inc.
Human Otc Drug
NDC 50845-0248

Emf also known as Argentum Nitricum, Arnica Montana, Baptisia Tinctoria, Cinchona Officinalis, Galium Aparine, Hepar Suis, Natrum Carbonicum, Panax Ginseng, Phosphoricum Acidum, Phosphorus, Rhododendron Chrysanthum, Strontium Carbonicum, Sulphur Iodatum, Thuja Occidentalis, X-ray is a human otc drug labeled by 'Liddell Laboratories, Inc.'. National Drug Code (NDC) number for Emf is 50845-0248. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Emf drug includes Alcohol, X-ray Exposed (1000 Rad) - 200 [hp_C]/mL Arnica Montana - 3 [hp_X]/mL Asian Ginseng - 1 [hp_X]/mL Baptisia Tinctoria Root - 3 [hp_X]/mL Cinchona Officinalis Bark - 6 [hp_X]/mL Galium Aparine - 3 [hp_X]/mL Phosphoric Acid - 3 [hp_X]/mL Phosphorus - 12 [hp_X]/mL Pork Liver - 6 [hp_X]/mL Rhododendron Aureum Leaf - 30 [hp_C]/mL and more. The currest status of Emf drug is Active.

Drug Information:

Drug NDC:	50845-0248
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:	Emf
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:	Argentum Nitricum, Arnica Montana, Baptisia Tinctoria, Cinchona Officinalis, Galium Aparine, Hepar Suis, Natrum Carbonicum, Panax Ginseng, Phosphoricum Acidum, Phosphorus, Rhododendron Chrysanthum, Strontium Carbonicum, Sulphur Iodatum, Thuja Occidentalis, X-ray
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Liddell Laboratories, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Spray
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:	ALCOHOL, X-RAY EXPOSED (1000 RAD) - 200 [hp_C]/mL ARNICA MONTANA - 3 [hp_X]/mL ASIAN GINSENG - 1 [hp_X]/mL BAPTISIA TINCTORIA ROOT - 3 [hp_X]/mL CINCHONA OFFICINALIS BARK - 6 [hp_X]/mL GALIUM APARINE - 3 [hp_X]/mL PHOSPHORIC ACID - 3 [hp_X]/mL PHOSPHORUS - 12 [hp_X]/mL PORK LIVER - 6 [hp_X]/mL RHODODENDRON AUREUM LEAF - 30 [hp_C]/mL Load more... SILVER NITRATE - 30 [hp_C]/mL SODIUM CARBONATE - 200 [hp_C]/mL STRONTIUM CARBONATE - 12 [hp_X]/mL SULFUR IODIDE - 200 [hp_C]/mL THUJA OCCIDENTALIS LEAFY TWIG - 200 [hp_C]/mL
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:	30 Jan, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	09 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:	Liddell Laboratories, Inc.
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.
UNII:	6PRJ93602P O80TY208ZW CUQ3A77YXI 5EF0HWI5WU S003A158SB Z4B6561488 E4GA8884NN 27YLU75U4W 6EC706HI7F IV92NQJ73U Load more... 95IT3W8JZE 45P3261C7T 41YPU4MMCA L6L8KA2AA0 1NT28V9397
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.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
50845-0248-1	30 mL in 1 BOTTLE, SPRAY (50845-0248-1)	30 Jan, 2019	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

Emf

Argentum Nitricum & more..

Spray
Liddell Laboratories, Inc.
NDC: 50845-0248

Purpose:

Uses: may temporarily aid in detoxifying the body and temporarily relieve symptoms of electromagnetic field (emf) radiation exposure, such as: recurring fatigue nausea disturbed sleep frequent headaches mental confusion** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

Emf argentum nitricum, arnica montana, baptisia tinctoria, cinchona officinalis, galium aparine, hepar suis, natrum carbonicum, panax ginseng, phosphoricum acidum, phosphorus, rhododendron chrysanthum, strontium carbonicum, sulphur iodatum, thuja occidentalis, x-ray silver nitrate silver cation arnica montana arnica montana baptisia tinctoria root baptisia tinctoria root cinchona officinalis bark cinchona officinalis bark galium aparine galium aparine pork liver pork liver sodium carbonate carbonate ion asian ginseng asian ginseng phosphoric acid phosphoric acid phosphorus phosphorus rhododendron aureum leaf rhododendron aureum leaf strontium carbonate strontium cation sulfur iodide sulfur iodide thuja occidentalis leafy twig thuja occidentalis leafy twig alcohol, x-ray exposed (1000 rad) alcohol, x-ray exposed (1000 rad) water alcohol

Indications and Usage:

Indications: may temporarily aid in detoxifying the body and temporarily relieve symptoms of electromagnetic field (emf) radiation exposure, such as: recurring fatigue nausea disturbed sleep frequent headaches mental confusion** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Warnings:

Warnings: do not use if you have ever had an allergic reaction to this product or any of its ingredients. stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur. keep out of reach of children. in case of overdose, get medical help or call a poison control center right away. if pregnant or breast feeding, ask a doctor before using product. do not use if tamper evident seal around neck of bottle is missing or broken. store at room temperature.

Dosage and Administration:

Directions: adults and children over 12: spray twice under the tongue three times per day for one month. for the next three months use same dosage one week per month. children 12 and under: consult a doctor prior to use.

Package Label Principal Display Panel:

Package label display: oral sprays liddell laboratories est. 1994 detox 48 emf electromagnetic radiation may relieve symptoms of emf radiation: fatigue, headache, disturbed sleep, confusion. homeopathic doctor formulated readily absorbed. safe. no known side effects. easy to use. 1.0 fl oz (30 ml) emf emf

Further Questions:

Questions: dist. by liddell laboratories 201 apple blvd. woodbine, ia 51579 www.liddell.net 1-800-460-7733

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.