NDC 43742-0857 Osteoreg

Asafoetida, Kali Iodatum, Natrum Sulphuricum, Stillingia Sylvatica, Aranea Diadema, Vitamin D3, Hydrocortisone (cortisol), Mercurius Praecipitatus Ruber, Calcarea Phosphorica, Hekla Lava, Parathyroid Gland (bovine), Aurum Metallicum, Lycopodium Clavatum, Gaertner Bacillus (bach)

NDC Product Code 43742-0857

NDC CODE: 43742-0857

Proprietary Name: Osteoreg 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: Asafoetida, Kali Iodatum, Natrum Sulphuricum, Stillingia Sylvatica, Aranea Diadema, Vitamin D3, Hydrocortisone (cortisol), Mercurius Praecipitatus Ruber, Calcarea Phosphorica, Hekla Lava, Parathyroid Gland (bovine), Aurum Metallicum, Lycopodium Clavatum, Gaertner Bacillus (bach) 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Potassium iodide is used to loosen and break up mucus in the airways. This helps you cough up the mucus so you can breathe more easily if you have long-term lung problems (e.g., asthma, chronic bronchitis, emphysema). This medication is known as an expectorant. Potassium iodide is also used along with antithyroid medicines to prepare the thyroid gland for surgical removal, to treat certain overactive thyroid conditions (hyperthyroidism), and to protect the thyroid in a radiation exposure emergency. It works by shrinking the size of the thyroid gland and decreasing the amount of thyroid hormones produced. In a radiation emergency, potassium iodide blocks only the thyroid from absorbing radioactive iodine, protecting it from damage and reducing the risk of thyroid cancer. Use this medication along with other emergency measures that will be recommended to you by public health and safety officials (e.g., finding safe shelter, evacuation, controlling food supply).
  • This medication is used to treat a variety of skin conditions (e.g., insect bites, poison oak/ivy, eczema, dermatitis, allergies, rash, itching of the outer female genitals, anal itching). Hydrocortisone reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a mild corticosteroid.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-0857-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Osteoreg with NDC 43742-0857 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Osteoreg is asafoetida, kali iodatum, natrum sulphuricum, stillingia sylvatica, aranea diadema, vitamin d3, hydrocortisone (cortisol), mercurius praecipitatus ruber, calcarea phosphorica, hekla lava, parathyroid gland (bovine), aurum metallicum, lycopodium clavatum, gaertner bacillus (bach). 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.

Osteoreg 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.

  • ASAFETIDA 4 [hp_X]/mL
  • POTASSIUM IODIDE 4 [hp_X]/mL
  • SODIUM SULFATE 4 [hp_X]/mL
  • STILLINGIA SYLVATICA ROOT 4 [hp_X]/mL
  • ARANEUS DIADEMATUS 6 [hp_X]/mL
  • CHOLECALCIFEROL 6 [hp_X]/mL
  • HYDROCORTISONE 6 [hp_X]/mL
  • MERCURIC OXIDE 8 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 8 [hp_X]/mL
  • HEKLA LAVA 8 [hp_X]/mL
  • BOS TAURUS PARATHYROID GLAND 8 [hp_X]/mL
  • GOLD 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [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.
  • 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: 09-21-2016 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: 12-31-2020 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.

Osteoreg Product Label Images

Osteoreg 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:

Asafoetida 4X, Kali Iodatum 4X, Natrum Sulphuricum 4X, Stillingia Sylvatica 4X, Aranea Diadema 6X, Vitamin D3 6X, Hydrocortisone (Cortisol) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Mercurius Praecipitatus Ruber 8X, Calcarea Phosphorica 8X, 12X, 30X, 200X, Hekla Lava 8X, 12X, 30X, 200X, Parathyroid Gland (Bovine) 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Aurum Metallicum 12X, Lycopodium Clavatum 30X, Gaertner Bacillus (Bach) 30C.

Homeopathic Indications:

For the temporary relief of aches, pains, and swelling in teeth, and joints.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of aches, pains, and swelling in teeth, and joints.****These statements are based upon traditional 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:

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 43742-0512-1HOMEOPATHICOSTEOREG1 FL OZ (30 ml)

* Please review the disclaimer below.