NDC 58264-0202 N-4

Chelidonium Majus, Bryonia Alba Root, Strychnos Nux-vomica Seed, Lycopodium Clavatum Whole, Mammal Liver, Sodium Sulfate, And Milk Thistle

NDC Product Code 58264-0202

NDC Code: 58264-0202

Proprietary Name: N-4 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: Chelidonium Majus, Bryonia Alba Root, Strychnos Nux-vomica Seed, Lycopodium Clavatum Whole, Mammal Liver, Sodium Sulfate, And Milk Thistle 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.


Code Structure
  • 58264 - Dna Labs, Inc.
    • 58264-0202 - N-4

NDC 58264-0202-1

Package Description: 29.57 mL in 1 BOTTLE, GLASS

NDC Product Information

N-4 with NDC 58264-0202 is a a human over the counter drug product labeled by Dna Labs, Inc.. The generic name of N-4 is chelidonium majus, bryonia alba root, strychnos nux-vomica seed, lycopodium clavatum whole, mammal liver, sodium sulfate, and milk thistle. The product's dosage form is solution and is administered via sublingual form.

Labeler Name: Dna Labs, Inc.

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

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.


N-4 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.

  • CHELIDONIUM MAJUS 4 [hp_X]/mL
  • BRYONIA ALBA ROOT 4 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/mL
  • LYCOPODIUM CLAVATUM WHOLE 4 [hp_X]/mL
  • MAMMAL LIVER 200 [hp_X]/mL
  • SODIUM SULFATE 4 [hp_X]/mL
  • MILK THISTLE 4 [hp_X]/mL

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)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

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

  • Sublingual - Administration beneath the tongue.

Product Labeler Information

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

* Please review the disclaimer below.

N-4 Product Label Images

N-4 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

Other

NDC 58264-0202-1

  • Use only if cap seal is unbroken.

To be used according to standard homeopathic indications.

Otc - Purpose

Support for the Liver, Gallbladder, Digestion.

Inactive Ingredient

Chelidonium majus 4x, Bryonia 4x, Nux vomica 6x, Lycopodium clavatum 4x, Liver 6/12/30/60/200x, Natrum sulphuricum 4x, Carduus marianus 4x, 20% alcohol in purified water.

Suggested Dosage

One dropper under tongue two times daily. Acute symptoms ½ dropper under tongue every 30 minutes for two hours.

Storage And Handling

SHAKE WELL

Otc - Pregnancy Or Breast Feeding

  • As with drugs if you are pregnant or nursing a baby seek professional advice before using this product.

Otc - Keep Out Of Reach Of Children

  • Keep this and all medication out of the reach of children.

* Please review the disclaimer below.

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