Lymph 1

Alcohol, Fumaria Officinalis Flowering Top, Calcium Sulfide, Bos Taurus Lymph, Sus Scrofa Lymph, Pinus Sylvestris Leafy Twig, Green Peppercorn, Prunus Spinosa Flower Bud, Silicon Dioxide, Bos Taurus Spleen, Sus Scrofa Spleen, Sulfuric Acid

Viatrexx Bio Incorporated
Human Otc Drug
NDC 63776-310

Lymph 1 also known as Alcohol, Fumaria Officinalis Flowering Top, Calcium Sulfide, Bos Taurus Lymph, Sus Scrofa Lymph, Pinus Sylvestris Leafy Twig, Green Peppercorn, Prunus Spinosa Flower Bud, Silicon Dioxide, Bos Taurus Spleen, Sus Scrofa Spleen, Sulfuric Acid is a human otc drug labeled by 'Viatrexx Bio Incorporated'. National Drug Code (NDC) number for Lymph 1 is 63776-310. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Lymph 1 drug includes Alcohol - 30 [kp_C]/mL Bos Taurus Lymph - 200 [kp_C]/mL Bos Taurus Spleen - 200 [kp_C]/mL Calcium Sulfide - 30 [kp_C]/mL Fumaria Officinalis Flowering Top - 30 [kp_C]/mL Green Peppercorn - 30 [kp_C]/mL Pinus Sylvestris Leafy Twig - 30 [kp_C]/mL Potassium Carbonate - 30 [kp_C]/mL Prunus Spinosa Flower Bud - 30 [kp_C]/mL Silicon Dioxide - 200 [kp_C]/mL and more. The currest status of Lymph 1 drug is Active.

Drug Information:

Drug NDC:	63776-310
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:	Lymph 1
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:	Alcohol, Fumaria Officinalis Flowering Top, Calcium Sulfide, Bos Taurus Lymph, Sus Scrofa Lymph, Pinus Sylvestris Leafy Twig, Green Peppercorn, Prunus Spinosa Flower Bud, Silicon Dioxide, Bos Taurus Spleen, Sus Scrofa Spleen, Sulfuric Acid
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Viatrexx Bio Incorporated
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 - 30 [kp_C]/mL BOS TAURUS LYMPH - 200 [kp_C]/mL BOS TAURUS SPLEEN - 200 [kp_C]/mL CALCIUM SULFIDE - 30 [kp_C]/mL FUMARIA OFFICINALIS FLOWERING TOP - 30 [kp_C]/mL GREEN PEPPERCORN - 30 [kp_C]/mL PINUS SYLVESTRIS LEAFY TWIG - 30 [kp_C]/mL POTASSIUM CARBONATE - 30 [kp_C]/mL PRUNUS SPINOSA FLOWER BUD - 30 [kp_C]/mL SILICON DIOXIDE - 200 [kp_C]/mL Load more... SULFURIC ACID - 30 [kp_C]/mL SUS SCROFA LYMPH - 200 [kp_C]/mL SUS SCROFA SPLEEN - 200 [kp_C]/mL TILIA TOMENTOSA BUD - 30 [kp_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:	24 Jul, 2012
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	18 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:	VIATREXX BIO INCORPORATED
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:	3K9958V90M UGE0WQC19W 190Q9MB3U3 1MBW07J51Q VH659J61ZL 6G53L8ESRK Q1RGP4UB73 BQN1B9B9HA 53Y84VPS2W ETJ7Z6XBU4 Load more... O40UQP6WCF 33A7VYU29L 92AMN5J79Y Z092RFX1IW
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
63776-310-15	1 BOTTLE, SPRAY in 1 BOX (63776-310-15) / 50 mL in 1 BOTTLE, SPRAY	24 Jul, 2012	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

Lymph 1

Alcohol & more..

Spray
VIATREXX BIO INCORPORATED
NDC: 63776-310

Purpose:

Purpose: ethylicum drainage fumaria off drainage hepar sulphuris calc drainage kali carb drainage lymph node lymph support pinus sylvestris drainage piper nigrum drainage prunus spinosa drainage silicia drainage spleen immune support sulphuricum acidum drainage tilia tomentosa neurological

Product Elements:

Lymph 1 alcohol, fumaria officinalis flowering top, calcium sulfide, bos taurus lymph, sus scrofa lymph, pinus sylvestris leafy twig, green peppercorn, prunus spinosa flower bud, silicon dioxide, bos taurus spleen, sus scrofa spleen, sulfuric acid water alcohol alcohol fumaria officinalis flowering top fumaria officinalis flowering top calcium sulfide calcium sulfide potassium carbonate carbonate ion bos taurus lymph bos taurus lymph pinus sylvestris leafy twig pinus sylvestris leafy twig sus scrofa lymph sus scrofa lymph green peppercorn green peppercorn prunus spinosa flower bud prunus spinosa flower bud silicon dioxide silicon dioxide bos taurus spleen bos taurus spleen sus scrofa spleen sus scrofa spleen sulfuric acid sulfuric acid tilia tomentosa bud tilia tomentosa bud

Indications and Usage:

Uses to help support the structure & function of the of the lymphatic system

Warnings:

Warnings stop use and ask a health care practitioner if symptoms persist for more than five days or worsen. if pregnant or breastfeeding, ask a health care practitioner before use.

Dosage and Administration:

Dosage 1-3 spray(s); 1-3 time(s) per day or as recommended by your health care practitioner.

Package Label Principal Display Panel:

Principal display panel item: vpc0370 ndc 63776-310-15 homeopathic remedy lymph 1 â¢ to help support the structure & function of the of the lymphatic system oral spray 50ml 1.7 oz viatrexx â¢ bio incorporated manufactured by viatrexx www.viatrexx.com newark, de 19713 lymph 1 50 ml 1.7 oz viatrexx â¢ bio incorporated item: vpc0370 ndc: 63776-310-15 indications: to help support the structure & function of the lymphatic system. directions: 1-3 spray(s); 1-3 time(s) per day or as recommended by your health care practitioner. mfg. for viatrexx bio incorporated. www.viatrexx.com newark, de 19713 lymph 1 carton ingredients

Further Questions:

Questions info@viatrexx.com

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.