NDC 61657-0526 Met-tox

Arsenicum Album, Avena Sativa, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Phytolacca Decandrarhamnus Frangula, Solidago Virgaurea, Trifolium Pratense, Heavy Metal Nosodes

NDC Product Code 61657-0526

NDC CODE: 61657-0526

Proprietary Name: Met-tox What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Arsenicum Album, Avena Sativa, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Phytolacca Decandrarhamnus Frangula, Solidago Virgaurea, Trifolium Pratense, Heavy Metal Nosodes What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Arsenic trioxide is used to treat a type of leukemia (acute promyelocytic leukemia-APL).
  • This product is used to treat dryness inside the nose (nasal passages). It helps add moisture inside the nose to dissolve and soften thick or crusty mucus. In babies and young children with stuffy noses who cannot blow their noses, using this product helps to make the mucus easier to remove with a nasal bulb syringe. This helps relieve stuffiness and makes breathing easier. This product contains a purified gentle salt solution (also called saline or sodium chloride solution). It does not contain any medication.
  • This medication is an iron supplement used to treat or prevent low blood levels of iron (e.g., for anemia or during pregnancy). Iron is an important mineral that the body needs to produce red blood cells and keep you in good health.
  • This medication is a mineral supplement used to prevent and treat low amounts of magnesium in the blood. Some brands are also used to treat symptoms of too much stomach acid such as stomach upset, heartburn, and acid indigestion. Magnesium is very important for the normal functioning of cells, nerves, muscles, bones, and the heart. Usually, a well-balanced diet provides normal blood levels of magnesium. However, certain situations cause your body to lose magnesium faster than you can replace it from your diet. These situations include treatment with water pills (diuretics such as furosemide, hydrochlorothiazide), a poor diet, alcoholism, or other medical conditions (e.g., severe diarrhea/vomiting, stomach/intestinal absorption problems, poorly controlled diabetes).
  • Drug uses not available
  • This medication is used to prevent or treat low blood calcium levels in people who do not get enough calcium from their diets. It may be used to treat conditions caused by low calcium levels such as bone loss (osteoporosis), weak bones (osteomalacia/rickets), decreased activity of the parathyroid gland (hypoparathyroidism), and a certain muscle disease (latent tetany). It may also be used in certain patients to make sure they are getting enough calcium (e.g., women who are pregnant, nursing, or postmenopausal, people taking certain medications such as phenytoin, phenobarbital, or prednisone). Calcium plays a very important role in the body. It is necessary for normal functioning of nerves, cells, muscle, and bone. If there is not enough calcium in the blood, then the body will take calcium from bones, thereby weakening bones. Having the right amount of calcium is important for building and keeping strong bones.
  • Drug uses not available
  • Drug uses not available
  • Drug uses not available
  • This medication is used to treat manic-depressive disorder (bipolar disorder). It works to stabilize the mood and reduce extremes in behavior by restoring the balance of certain natural substances (neurotransmitters) in the brain. Some of the benefits of continued use of this medication include decreasing how often manic episodes occur and decreasing the symptoms of manic episodes, such as exaggerated feelings of well-being, feelings that others wish to harm you, irritability, anxiousness, rapid/loud speech, and aggressive/hostile behaviors.
  • Drug uses not available

NDC Code Structure

  • 61657 - White Manufacturing Inc Dba Micro-west

NDC 61657-0526-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Met-tox with NDC 61657-0526 is a a human over the counter drug product labeled by White Manufacturing Inc Dba Micro-west. The generic name of Met-tox is arsenicum album, avena sativa, lycopodium clavatum, natrum muriaticum, nux vomica, phytolacca decandrarhamnus frangula, solidago virgaurea, trifolium pratense, heavy metal nosodes. The product's dosage form is liquid and is administered via oral form.

Labeler Name: White Manufacturing Inc Dba Micro-west

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates 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.

Met-tox Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ARSENIC TRIOXIDE 12 [hp_X]/30mL
  • AVENA SATIVA FLOWERING TOP 3 [hp_X]/30mL
  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/30mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/30mL
  • SODIUM CHLORIDE 12 [hp_X]/30mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/30mL
  • PHYTOLACCA AMERICANA ROOT 3 [hp_X]/30mL
  • FRANGULA ALNUS BARK 3 [hp_X]/30mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 3 [hp_X]/30mL
  • TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/30mL
  • IRON 12 [hp_X]/30mL
  • MAGNESIUM 12 [hp_X]/30mL
  • SULFUR 12 [hp_X]/30mL
  • CHROMIUM 12 [hp_X]/30mL
  • ALUMINUM 12 [hp_X]/30mL
  • CALCIUM 12 [hp_X]/30mL
  • ACTIVATED CHARCOAL 12 [hp_X]/30mL
  • SILICON 12 [hp_X]/30mL
  • SELENIUM 12 [hp_X]/30mL
  • ZINC 12 [hp_X]/30mL
  • BORON 12 [hp_X]/30mL
  • COBALT 12 [hp_X]/30mL
  • BERYLLIUM 12 [hp_X]/30mL
  • TIN 12 [hp_X]/30mL
  • ANTIMONY 12 [hp_X]/30mL
  • CERIUM 12 [hp_X]/30mL
  • CESIUM 12 [hp_X]/30mL
  • ARSENIC 12 [hp_X]/30mL
  • ZIRCONIUM 12 [hp_X]/30mL
  • STRONTIUM 12 [hp_X]/30mL
  • NEODYMIUM 12 [hp_X]/30mL
  • LEAD 12 [hp_X]/30mL
  • CHLORIDE ION 12 [hp_X]/30mL
  • LITHIUM 12 [hp_X]/30mL
  • COPPER 12 [hp_X]/30mL
  • BROMINE 12 [hp_X]/30mL
  • SODIUM 12 [hp_X]/30mL
  • YTTRIUM 12 [hp_X]/30mL
  • IODINE 12 [hp_X]/30mL
  • GADOLINIUM 12 [hp_X]/30mL
  • FLUORIDE ION 12 [hp_X]/30mL
  • SAMARIUM 12 [hp_X]/30mL
  • CADMIUM 12 [hp_X]/30mL
  • DYSPROSIUM 12 [hp_X]/30mL
  • MERCURY 12 [hp_X]/30mL
  • TITANIUM 12 [hp_X]/30mL
  • POTASSIUM 12 [hp_X]/30mL
  • RUBIDIUM 12 [hp_X]/30mL
  • ERBIUM 12 [hp_X]/30mL
  • VANADIUM 12 [hp_X]/30mL
  • SCANDIUM 12 [hp_X]/30mL
  • RUTHENIUM 12 [hp_X]/30mL
  • LUTETIUM 12 [hp_X]/30mL
  • HOLMIUM 12 [hp_X]/30mL
  • PRASEODYMIUM 12 [hp_X]/30mL
  • TERBIUM 12 [hp_X]/30mL
  • BARIUM 12 [hp_X]/30mL
  • TELLURIUM 12 [hp_X]/30mL
  • NIOBIUM 12 [hp_X]/30mL
  • PALLADIUM 12 [hp_X]/30mL
  • HAFNIUM 12 [hp_X]/30mL
  • TANTALUM 12 [hp_X]/30mL
  • MOLYBDENUM 12 [hp_X]/30mL
  • EUROPIUM 12 [hp_X]/30mL
  • GALLIUM 12 [hp_X]/30mL
  • GOLD 12 [hp_X]/30mL
  • OSMIUM 12 [hp_X]/30mL
  • PLATINUM 12 [hp_X]/30mL
  • RHODIUM 12 [hp_X]/30mL
  • INDIUM 12 [hp_X]/30mL
  • SILVER 12 [hp_X]/30mL
  • THORIUM 12 [hp_X]/30mL
  • IRIDIUM 12 [hp_X]/30mL
  • HYDROGEN 12 [hp_X]/30mL
  • NITROGEN 12 [hp_X]/30mL
  • YTTERBIUM 12 [hp_X]/30mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: White Manufacturing Inc Dba Micro-west
Labeler Code: 61657
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product 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.

Start Marketing Date: 01-24-2006 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Met-tox Product Label Images

Met-tox Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

ARSENICUM ALBUM 12XAVENA SATIVA 3XBERBERIS VULGARIS 3XLYCOPODIUM CLAVATUM 12XNATRUM MURIATICUM 12XNUX VOMICA 12XPHYTOLACCA DECANDRA 3XRHAMNUS FRANGULA 3XSOLIDAGO VIRGAUREA 3XTRIFOLIUM PRATENSE 3X

Otc - Purpose

FOR THE TEMPORARY RELIEF OF EXHAUSTION, WEAKNESS, ACHING, SORENESS AND RESTLESSNESS

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Other Information

TAMPER RESISTANT FOR YOUR PROTECTION. USE ONLY IF SEAL IS INTACT

Indications & Usage

INDICATIONS: FOR THE TEMPORARY RELIEF OF EXHAUSTION, WEAKNESS, ACHING, SORENESS AND RESTLESSNESS

Warnings

WARNING:STOP USE AND CALL A DOCTOR IF SYMPTOMS PERSIST OR WORSEN. IF PREGNANT OR BREAST FEEDING, CONSULT A HEALTHCARE PROFESSIONAL BEFORE USE. CONTAINS ALCOHOL: IN CASE OF ACCIDENTAL OVERDOSE, CONSULT A POISON CONTROL CENTER IMMEDIATELY

Directions

DIRECTIONS:TAKE 6 DROPS ORALLY, 4 TIMES A DAY. FOR AGES 2 TO ADULT

Inactive Ingredient

ALCOHOL (20% V/V) PURIFIED WATER

Manufacture

MANUFACTURED FOR MICRO-WESTP.O. BOX 950DOUGLAS, WY 826331-307-358-5066

* Please review the disclaimer below.