NDC 43689-0022 Muscle Cramp Pain Reliever

Causticum, Colocynthis, Cuprum Metallicum, Magnesia Phosphorica, Phytolacca Decandra, Rhus Tox, Stannum Metallicum, Veratrum Album

NDC Product Code 43689-0022

NDC Code: 43689-0022

Proprietary Name: Muscle Cramp Pain Reliever 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: Causticum, Colocynthis, Cuprum Metallicum, Magnesia Phosphorica, Phytolacca Decandra, Rhus Tox, Stannum Metallicum, Veratrum Album 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.

NDC Code Structure

  • 43689 - The Magni Company

NDC 43689-0022-2

Package Description: 1 BOTTLE in 1 CARTON > 125 TABLET in 1 BOTTLE (43689-0022-1)

NDC Product Information

Muscle Cramp Pain Reliever with NDC 43689-0022 is a a human over the counter drug product labeled by The Magni Company. The generic name of Muscle Cramp Pain Reliever is causticum, colocynthis, cuprum metallicum, magnesia phosphorica, phytolacca decandra, rhus tox, stannum metallicum, veratrum album. The product's dosage form is tablet and is administered via oral form.

Labeler Name: The Magni Company

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

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.

Muscle Cramp Pain Reliever 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.

  • CAUSTICUM 12 [hp_X]/1
  • CITRULLUS COLOCYNTHIS FRUIT PULP 12 [hp_X]/1
  • COPPER 12 [hp_X]/1
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 12 [hp_X]/1
  • PHYTOLACCA AMERICANA ROOT 12 [hp_X]/1
  • TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/1
  • TIN 12 [hp_X]/1
  • VERATRUM ALBUM ROOT 12 [hp_X]/1

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.

  • LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)

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.

Product Labeler Information

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

Labeler Name: The Magni Company
Labeler Code: 43689
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: 09-18-2019 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.

Muscle Cramp Pain Reliever 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

Causticum, Colocynthis, Cuprum Metallicum, Magnesia Phosphorica, Phytolacca Decandra, Rhus Tox, Stannum Metallicum, Veratrum Album

Indications

Temporarily relieves the symptoms of pain, stiffness and cramping in joints, legs, feet, hips and back.

Warnings

If pregnant or breastfeeding, ask a health professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Is symptoms persist for more than 7 days or worsens, consult your physician.

Keep Out Of Reach Of Children

In case of overdose, get medical help or contact a Poison Control Center right away. If symptoms persist for more than 7 days or worsens, consult your physician.

Directions

Adults and children 12 years and above, dissolve 2 tablets under tongue 2 to 3 times daily or as directed by a physician.Children under 12 years of age, consult a physician. Take at least 10 minutes before or after eating or drinking.

Indications And Usage

Temporarily relieves the symptoms of pain, stiffness and cramping in joints, legs, hips and back.

Inactive Ingredients

Lactose, Magnesium Stearate, Microcrystalline Cellulose.

Questions

Dist. by:The Magni Group, Inc. McKinney, TX 75071 USAwww.magnilife.com 1-800-645-9199

Package Label:

MAGNILIFEHomeopathicNDC 43689-0022-1MUSCLE CRAMP PAIN RELIEVERFor relief of muscle pain, cramping and stiffness,√Legs√Feet√Back√Hips√Joints125 Dissolving Tablets

* Please review the disclaimer below.