NDC 43857-0487 Additox

Trifolium Pratense, Xanthoxylum Fraxineum, Phytolacca Decandra, Arsenicum Album, Belladonna, Chelidonium Majus, Lycopodium Clavatum, Phosphoricum Acidum, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methylparaben, Propylparaben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum

NDC Product Code 43857-0487

NDC Code: 43857-0487

Proprietary Name: Additox 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: Trifolium Pratense, Xanthoxylum Fraxineum, Phytolacca Decandra, Arsenicum Album, Belladonna, Chelidonium Majus, Lycopodium Clavatum, Phosphoricum Acidum, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methylparaben, Propylparaben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum 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
  • 43857 - Bioactive Nutritional, Inc.
    • 43857-0487 - Additox

NDC 43857-0487-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Additox with NDC 43857-0487 is a a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Additox is trifolium pratense, xanthoxylum fraxineum, phytolacca decandra, arsenicum album, belladonna, chelidonium majus, lycopodium clavatum, phosphoricum acidum, aspartame, benzalkonium chloride, formalinum, methylene chloride, methylparaben, propylparaben, sodium benzoate, sodium citrate, titanium dioxide, zincum oxydatum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Bioactive Nutritional, 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.


Additox 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.

  • TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
  • ZANTHOXYLUM AMERICANUM BARK 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
  • ARSENIC TRIOXIDE 12 [hp_X]/mL
  • ATROPA BELLADONNA 12 [hp_X]/mL
  • CHELIDONIUM MAJUS 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • ASPARTAME 30 [hp_X]/mL
  • BENZALKONIUM CHLORIDE 30 [hp_X]/mL
  • FORMALDEHYDE 30 [hp_X]/mL
  • METHYLENE CHLORIDE 30 [hp_X]/mL
  • METHYLPARABEN 30 [hp_X]/mL
  • PROPYLPARABEN 30 [hp_X]/mL
  • SODIUM BENZOATE 30 [hp_X]/mL
  • SODIUM CITRATE 30 [hp_X]/mL
  • TITANIUM DIOXIDE 30 [hp_X]/mL
  • ZINC OXIDE 30 [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.

  • 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.

* Please review the disclaimer below.

Additox Product Label Images

Additox 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:

Trifolium Pratense 3X, Xanthoxylum Fraxineum 3X, Phytolacca Decandra 4X, Arsenicum Album 12X, Belladonna 12X, Chelidonium Majus 12X, Lycopodium Clavatum 12X, Phosphoricum Acidum 12X, Aspartame 30X, Benzalkonium Chloride 30X, Formalinum 30X, Methylene Chloride 30X, Methylparaben 30X, Propylparaben 30X, Sodium Benzoate 30X, Sodium Citrate 30X, Titanium Dioxide 30X.

Indications:

For temporary relief of debility, exhaustion, exhaustion after slight exertion, and dysentery.

For temporary relief of debility, exhaustion, exhaustion after slight exertion, and dysentery.

Warnings:

If pregnant or breast-feeding, ask a health care professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store in cool, dry place.

Directions:

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol.

Demineralized Water, 25% Ethanol.

Questions:

Distributed by:BioActive Nutritional, Inc.1803 N. Wickham Rd.Melbourne, FL 32935bioactivenutritional.com*For a complete list of Addisodes contact BioActive Nutritional, Inc.

Package Label Display:

BIOActive NutritionalADDITOXHOMEOPATHIC1 FL OZ (30 ml)

* Please review the disclaimer below.

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