NDC 43742-1120 Addiclenz
Beta Vulgaris, Boldo, Chelidonium Majus, Petroselinum Sativum, Taraxacum Officinale, Arsenicum Album, Bisphenol A, Cobaltum Metallicum, Cuprum Metallicum, Glyphosate, Iodium, Lycopodium Clavatum, Phosphoricum Acidum, Selenium Metallicum, Zincum Metallicum, Bacillus Thuringiensis (bt Toxin), Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methyl Paraben, Propyl Paraben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum
NDC Product Code 43742-1120
Proprietary Name: Addiclenz 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: Beta Vulgaris, Boldo, Chelidonium Majus, Petroselinum Sativum, Taraxacum Officinale, Arsenicum Album, Bisphenol A, Cobaltum Metallicum, Cuprum Metallicum, Glyphosate, Iodium, Lycopodium Clavatum, Phosphoricum Acidum, Selenium Metallicum, Zincum Metallicum, Bacillus Thuringiensis (bt Toxin), Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methyl Paraben, Propyl Paraben, 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
- 43742 - Deseret Biologicals, Inc.
- 43742-1120 - Addiclenz
NDC 43742-1120-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
NDC Product Information
Addiclenz with NDC 43742-1120 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Addiclenz is beta vulgaris, boldo, chelidonium majus, petroselinum sativum, taraxacum officinale, arsenicum album, bisphenol a, cobaltum metallicum, cuprum metallicum, glyphosate, iodium, lycopodium clavatum, phosphoricum acidum, selenium metallicum, zincum metallicum, bacillus thuringiensis (bt toxin), aspartame, benzalkonium chloride, formalinum, methylene chloride, methyl paraben, propyl paraben, sodium benzoate, sodium citrate, titanium dioxide, zincum oxydatum. The product's dosage form is liquid and is administered via oral form.
Labeler Name: Deseret Biologicals, 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.
Addiclenz 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.
- BETA VULGARIS 3 [hp_X]/mL
- PEUMUS BOLDUS LEAF 3 [hp_X]/mL
- CHELIDONIUM MAJUS 3 [hp_X]/mL
- PETROSELINUM CRISPUM 3 [hp_X]/mL
- TARAXACUM OFFICINALE 3 [hp_X]/mL
- ARSENIC TRIOXIDE 12 [hp_X]/mL
- BISPHENOL A 12 [hp_X]/mL
- COBALT 12 [hp_X]/mL
- COPPER 12 [hp_X]/mL
- GLYPHOSATE 12 [hp_X]/mL
- IODINE 12 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- PHOSPHORIC ACID 12 [hp_X]/mL
- SELENIUM 12 [hp_X]/mL
- ZINC 12 [hp_X]/mL
- BACILLUS THURINGIENSIS 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.
Labeler Code: 43742
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: 12-19-2017 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
End Marketing Date: 03-30-2023 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
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.
Addiclenz Product Label Images
Addiclenz 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:
- Homeopathic Indications:
- Warnings:
- Keep Out Of Reach Of Children:
- Directions:
- Inactive Ingredients:
- Questions:
- Package Label Display:
Active Ingredients:
Beta Vulgaris 3X, Boldo 3X, Chelidonium Majus 3X, Petroselinum Sativum 3X, Taraxacum Officinale 3X, Arsenicum Album 12X, Bisphenol A 12X, Cobaltum Metallicum 12X, Cuprum Metallicum 12X, Glyphosate 12X, Iodium 12X, Lycopodium Clavatum 12X, Phosphoricum Acidum 12X, Selenium Metallicum 12X, Zincum Metallicum 12X, Bacillus Thuringiensis (BT Toxin) 12X, 30X, 200X, Aspartame 30X, Benzalkonium Chloride 30X, Formalinum 30X, Methylene Chloride 30X, Methyl Paraben 30X, Propyl Paraben 30X, Sodium Benzoate 30X, Sodium Citrate 30X, Titanium Dioxide 30X, Zincum Oxydatum 30X.
Homeopathic Indications:
For temporary relief of symptoms related to food additives, herbicides and insecticides including muscle weakness, skin irritation, poor muscle coordination, headache, cough, diarrhea, dizziness, fatigue, fever, stomach pain and vomiting.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
For temporary relief of symptoms related to food additives, herbicides and insecticides including muscle weakness, skin irritation, poor muscle coordination, headache, cough, diarrhea, dizziness, fatigue, fever, stomach pain and vomiting.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Warnings:
Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.
Keep Out Of Reach Of Children:
Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.
Directions:
1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
Inactive Ingredients:
Demineralized Water, 25% Ethanol
Questions:
Dist. By: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070www.desbio.com*For a complete list of Addisode contact Deseret Biologicals, Inc.
Package Label Display:
DESBIONDC 43742-1120-1HOMEOPATHICADDICLENZ1 FL OZ (30 ml)
* Please review the disclaimer below.