NDC 43742-0579 Dairy Allergen Mix

Adenosinum Triphosphoricum Dinatrum, Apiolum, Benzoicum Acidum, Cholinum, Cinnamic Acid, Coumarinum, Eugenol, Folic Acid, Folliculinum, Formalinum, Gaba (gamma-aminobutyric Acid), Histaminum Hydrochloricum, L-asparagine (monohydrate), Lac Defloratum, Lac Vaccinum, Menadione, Oophorinum (suis), Phenyl Isothiocyanate, Quercetin, Rutin, Saccharum Lactis, Ileum (suis), Jejunum (suis), Stomach (suis), Sarcolacticum Acidum, Lac Caninum, Lac Felinum, Lac Humanum, Piperine, Calcarea Carbonica

NDC Product Code 43742-0579

NDC Code: 43742-0579

Proprietary Name: Dairy Allergen Mix 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: Adenosinum Triphosphoricum Dinatrum, Apiolum, Benzoicum Acidum, Cholinum, Cinnamic Acid, Coumarinum, Eugenol, Folic Acid, Folliculinum, Formalinum, Gaba (gamma-aminobutyric Acid), Histaminum Hydrochloricum, L-asparagine (monohydrate), Lac Defloratum, Lac Vaccinum, Menadione, Oophorinum (suis), Phenyl Isothiocyanate, Quercetin, Rutin, Saccharum Lactis, Ileum (suis), Jejunum (suis), Stomach (suis), Sarcolacticum Acidum, Lac Caninum, Lac Felinum, Lac Humanum, Piperine, Calcarea Carbonica 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

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-0579-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Dairy Allergen Mix with NDC 43742-0579 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Dairy Allergen Mix is adenosinum triphosphoricum dinatrum, apiolum, benzoicum acidum, cholinum, cinnamic acid, coumarinum, eugenol, folic acid, folliculinum, formalinum, gaba (gamma-aminobutyric acid), histaminum hydrochloricum, l-asparagine (monohydrate), lac defloratum, lac vaccinum, menadione, oophorinum (suis), phenyl isothiocyanate, quercetin, rutin, saccharum lactis, ileum (suis), jejunum (suis), stomach (suis), sarcolacticum acidum, lac caninum, lac felinum, lac humanum, piperine, calcarea carbonica. 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.

Dairy Allergen Mix 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.

  • ADENOSINE TRIPHOSPHATE DISODIUM 4 [hp_X]/mL
  • APIOLE (PARSLEY) 6 [hp_X]/mL
  • BENZOIC ACID 6 [hp_X]/mL
  • CHOLINE HYDROXIDE 6 [hp_X]/mL
  • CINNAMIC ACID 6 [hp_X]/mL
  • COUMARIN 6 [hp_X]/mL
  • EUGENOL 6 [hp_X]/mL
  • FOLIC ACID 6 [hp_X]/mL
  • ESTRONE 6 [hp_X]/mL
  • FORMALDEHYDE 6 [hp_X]/mL
  • .GAMMA.-AMINOBUTYRIC ACID 6 [hp_X]/mL
  • HISTAMINE DIHYDROCHLORIDE 6 [hp_X]/mL
  • ASPARAGINE MONOHYDRATE 6 [hp_X]/mL
  • SKIM MILK 6 [hp_X]/mL
  • COW MILK 6 [hp_X]/mL
  • MENADIONE 6 [hp_X]/mL
  • SUS SCROFA OVARY 6 [hp_X]/mL
  • PHENYL ISOTHIOCYANATE 6 [hp_X]/mL
  • QUERCETIN 6 [hp_X]/mL
  • RUTIN 6 [hp_X]/mL
  • LACTOSE 6 [hp_X]/mL
  • SUS SCROFA ILEUM 8 [hp_X]/mL
  • SUS SCROFA JEJUNUM 8 [hp_X]/mL
  • SUS SCROFA STOMACH 8 [hp_X]/mL
  • LACTIC ACID, L- 8 [hp_X]/mL
  • CANIS LUPUS FAMILIARIS MILK 30 [hp_X]/mL
  • FELIS CATUS MILK 30 [hp_X]/mL
  • HUMAN MILK 30 [hp_X]/mL
  • PIPERINE 30 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 6 [hp_C]/mL
  • CALCIUM FLUORIDE 6 [hp_C]/mL
  • TRIBASIC CALCIUM PHOSPHATE 6 [hp_C]/mL
  • ACTIVATED CHARCOAL 6 [hp_C]/mL
  • MATRICARIA RECUTITA 6 [hp_C]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 6 [hp_C]/mL
  • TOXICODENDRON PUBESCENS LEAF 6 [hp_C]/mL
  • CALCIUM CITRATE 6 [hp_C]/mL
  • CALCIUM GLUCONATE 6 [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: Deseret Biologicals, Inc.
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: 05-07-2015 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: 06-12-2023 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.

Dairy Allergen Mix Product Label Images

Dairy Allergen Mix 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:

Adenosinum Triphosphoricum Dinatrum 4X, Apiolum 6X, 10X, 30X, 200X, Benzoicum Acidum 6X, 10X, 30X, 200X, Cholinum 6X, 10X, 30X, 200X, Cinnamic Acid 6X, 10X, 30X, 200X, Coumarinum 6X, 10X, 30X, 200X, Eugenol 6X, 10X, 30X, 200X, Folic Acid 6X, 10X, 30X, 200X, Folliculinum 6X, 10X, 30X, 200X, Formalinum 6X, 10X, 30X, 200X, GABA (Gamma-Aminobutyric Acid) 6X, 10X, 30X, 200X, Histaminum Hydrochloricum 6X, 10X, 30X, 200X, L-Asparagine (Monohydrate) 6X, 10X, 30X, 200X, Lac Defloratum 6X, 10X, 30X, 200X, Lac Vaccinum 6X, 10X, 30X, 200X, Menadione 6X, 10X, 30X, 200X, Oophorinum (Suis) 6X, 10X, 30X, 200X, Phenyl Isothiocyanate 6X, 10X, 30X, 200X, Quercetin 6X, 10X, 30X, 200X, Rutin 6X, 10X, 30X, 200X, Saccharum Lactis 6X, 10X, 30X, 200X, Ileum (Suis) 8X, Jejunum (Suis) 8X, Stomach (Suis) 8X, Sarcolacticum Acidum 8X, 10X, 30X, 200X, Lac Caninum 30X, 200X, Lac Felinum 30X, 200X, Lac Humanum 30X, 200X, Piperine 30X, 200X, Calcarea Carbonica 6C, 30C, Calcarea Fluorica 6C, 30C, Calcarea Phosphorica 6C, 30C, Carbo Vegetabilis 6C, 30C, Chamomilla 6C, 30C, Gaertner Bacillus (Bach) 6C, 30C, Rhus Tox 6C, 30C, Calcium Citrate 6C, 30C, 200C, Calcium Gluconate 6C, 30C, 200C.

Indications:

For the temporary relief of symptoms of allergies to calcium in foods and supplements, including cramping of muscles, fatigue, and musculoskeletal weakness.

For the temporary relief of symptoms of allergies to calcium in foods and supplements, including cramping of muscles, fatigue, and musculoskeletal weakness.

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, get medical help or contact a Poison Control Center right away.

Directions:

3-10 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 84070 www.desbio.com

Package Label Display:

DESBIONDC 43742-0579-1HOMEOPATHICDAIRY ALLERGENMIX1 FL OZ (30 ml)

* Please review the disclaimer below.