NDC 43406-0641 Alumizen

Garlic, Avena Sativa Flowering Top, Berberis Vulgaris Root Bark, Arctium Lappa Root, Phytolacca Americana Root, Solidago Virgaurea Flowering Top, Aluminum Oxide, Silver Nitrate, Barium Carbonate, Beryllium, Cadmium, Copper, Hydrofluoric Acid, Indium, Iodine, Lithium Carbonate, Mercurius Solubilis, Nickel Carbonate Hydroxide Tetrahydrate, Nitrous Oxide, Lead, Selenium, Strontium Carbonate, Titanium, Arsenic Trioxide, Sodium Chloride, Strychnos Nux-vomica Seed.

NDC Product Code 43406-0641

NDC Code: 43406-0641

Proprietary Name: Alumizen 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: Garlic, Avena Sativa Flowering Top, Berberis Vulgaris Root Bark, Arctium Lappa Root, Phytolacca Americana Root, Solidago Virgaurea Flowering Top, Aluminum Oxide, Silver Nitrate, Barium Carbonate, Beryllium, Cadmium, Copper, Hydrofluoric Acid, Indium, Iodine, Lithium Carbonate, Mercurius Solubilis, Nickel Carbonate Hydroxide Tetrahydrate, Nitrous Oxide, Lead, Selenium, Strontium Carbonate, Titanium, Arsenic Trioxide, Sodium Chloride, Strychnos Nux-vomica Seed. 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

  • 43406 - Natural Creations, Inc.
    • 43406-0641 - Alumizen

NDC 43406-0641-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Alumizen with NDC 43406-0641 is a a human over the counter drug product labeled by Natural Creations, Inc.. The generic name of Alumizen is garlic, avena sativa flowering top, berberis vulgaris root bark, arctium lappa root, phytolacca americana root, solidago virgaurea flowering top, aluminum oxide, silver nitrate, barium carbonate, beryllium, cadmium, copper, hydrofluoric acid, indium, iodine, lithium carbonate, mercurius solubilis, nickel carbonate hydroxide tetrahydrate, nitrous oxide, lead, selenium, strontium carbonate, titanium, arsenic trioxide, sodium chloride, strychnos nux-vomica seed.. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Natural Creations, Inc.

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.

Alumizen 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.

  • GARLIC 6 [hp_X]/mL
  • AVENA SATIVA FLOWERING TOP 6 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 6 [hp_X]/mL
  • ARCTIUM LAPPA ROOT 6 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 6 [hp_X]/mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 6 [hp_X]/mL
  • ALUMINUM OXIDE 12 [hp_C]/mL
  • SILVER NITRATE 12 [hp_C]/mL
  • BARIUM CARBONATE 12 [hp_C]/mL
  • BERYLLIUM 12 [hp_C]/mL
  • CADMIUM 12 [hp_C]/mL
  • COPPER 12 [hp_C]/mL
  • HYDROFLUORIC ACID 12 [hp_C]/mL
  • INDIUM 12 [hp_C]/mL
  • IODINE 12 [hp_C]/mL
  • LITHIUM CARBONATE 12 [hp_C]/mL
  • MERCURIUS SOLUBILIS 12 [hp_C]/mL
  • NICKEL CARBONATE HYDROXIDE TETRAHYDRATE 12 [hp_C]/mL
  • NITROUS OXIDE 12 [hp_C]/mL
  • LEAD 12 [hp_C]/mL
  • SELENIUM 12 [hp_C]/mL
  • STRONTIUM CARBONATE 12 [hp_C]/mL
  • TITANIUM 12 [hp_C]/mL
  • ARSENIC TRIOXIDE 12 [hp_C]/mL
  • SODIUM CHLORIDE 12 [hp_C]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_C]/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.

  • WATER (UNII: 059QF0KO0R)
  • 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.

Product Labeler Information

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

Labeler Name: Natural Creations, Inc.
Labeler Code: 43406
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: 06-01-2016 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: 12-31-2019 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.

Alumizen Product Label Images

Alumizen 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

Otc - Active Ingredient

ACTIVE INGREDIENTS: Allium Sat 6X, Avena 6X, Berber Vulg 6X, Lappa 6X, Phytolacca 6X, Solidago 6X, Alumina 6C, 12C, Arg Nit 6C, 12C, Baryta Carb 6C, 12C, Beryllium 6C, 12C, Cadmium Met 6C, 12C, Cuprum Met 6C, 12C, Fluoricum Acidum 6C, 12C, Indium 6C, 12C, Iodium 6C, 12C, Lithium Carb 6C, 12C, Merc Solub 6C, 12C, Niccolum Carb 6C, 12C, Nitrogenum Oxygenatum 6C, 12C, Plumb Met 6C, 12C, Selenium 6C, 12C, Strontium Carb 6C, 12C, Titanium 6C, 12C, Arsenicum Alb 12C, Nat Mur 12C, Nux Vom 12C.

Otc - Purpose

USES: Temporarily relieves weakness and fatigue.**

Indications & Usage

USES: Temporarily relieves weakness and fatigue.**

Dosage & Administration

DIRECTIONS: Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

Warnings

WARNINGS:* Consult a physician for use in children under 12 years of age.* IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.* KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.* Do not use if TAMPER EVIDENT seal is broken or missing.

Inactive Ingredient

INACTIVE INGREDIENTS: Ethyl Alcohol USP, Purified Water.

Otc - Questions

QUESTIONS & COMMENTS?Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600

References

** These statements have not been reviewed by the FDA. They are based on traditional homeopathic practice.LOT:                                    NC726

* Please review the disclaimer below.

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