NDC 43742-1322 Pts/stress Remedy

Kali Phosphoricum, Ambra Grisea, Cacao, Phosphoricum Acidum, Arnica Montana, Calcarea Carbonica, Cerebrum Suis, Glandula Suprarenalis Suis, Lithium Carbonicum, Aconitum Napellus, Argemone Mexicana, Arsenicum Album, Cicuta Virosa, Hyoscyamus Niger, Ignatia Tigrinum, Natrum Muriaticum, Tarentula Hispanica, Stramonium, Buthus Australis

NDC Product Code 43742-1322

NDC CODE: 43742-1322

Proprietary Name: Pts/stress Remedy 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: Kali Phosphoricum, Ambra Grisea, Cacao, Phosphoricum Acidum, Arnica Montana, Calcarea Carbonica, Cerebrum Suis, Glandula Suprarenalis Suis, Lithium Carbonicum, Aconitum Napellus, Argemone Mexicana, Arsenicum Album, Cicuta Virosa, Hyoscyamus Niger, Ignatia Tigrinum, Natrum Muriaticum, Tarentula Hispanica, Stramonium, Buthus Australis 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.

  • This medication is used to treat manic-depressive disorder (bipolar disorder). It works to stabilize the mood and reduce extremes in behavior by restoring the balance of certain natural substances (neurotransmitters) in the brain. Some of the benefits of continued use of this medication include decreasing how often manic episodes occur and decreasing the symptoms of manic episodes, such as exaggerated feelings of well-being, feelings that others wish to harm you, irritability, anxiousness, rapid/loud speech, and aggressive/hostile behaviors.
  • Arsenic trioxide is used to treat a type of leukemia (acute promyelocytic leukemia-APL).
  • This product is used to treat dryness inside the nose (nasal passages). It helps add moisture inside the nose to dissolve and soften thick or crusty mucus. In babies and young children with stuffy noses who cannot blow their noses, using this product helps to make the mucus easier to remove with a nasal bulb syringe. This helps relieve stuffiness and makes breathing easier. This product contains a purified gentle salt solution (also called saline or sodium chloride solution). It does not contain any medication.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-1322-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Pts/stress Remedy with NDC 43742-1322 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Pts/stress Remedy is kali phosphoricum, ambra grisea, cacao, phosphoricum acidum, arnica montana, calcarea carbonica, cerebrum suis, glandula suprarenalis suis, lithium carbonicum, aconitum napellus, argemone mexicana, arsenicum album, cicuta virosa, hyoscyamus niger, ignatia tigrinum, natrum muriaticum, tarentula hispanica, stramonium, buthus australis. 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.

Pts/stress Remedy 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.

  • DIBASIC POTASSIUM PHOSPHATE 3 [hp_X]/mL
  • AMBERGRIS 6 [hp_X]/mL
  • COCOA 6 [hp_X]/mL
  • PHOSPHORIC ACID 6 [hp_X]/mL
  • ARNICA MONTANA 6 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X]/mL
  • SUS SCROFA CEREBRUM 8 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
  • LITHIUM CARBONATE 8 [hp_X]/mL
  • ACONITUM NAPELLUS 8 [hp_X]/mL
  • ARGEMONE MEXICANA 12 [hp_X]/mL
  • ARSENIC TRIOXIDE 12 [hp_X]/mL
  • CICUTA VIROSA ROOT 12 [hp_X]/mL
  • HYOSCYAMUS NIGER 12 [hp_X]/mL
  • STRYCHNOS IGNATII SEED 12 [hp_X]/mL
  • LILIUM LANCIFOLIUM WHOLE FLOWERING 12 [hp_X]/mL
  • SODIUM CHLORIDE 12 [hp_X]/mL
  • LYCOSA TARANTULA 12 [hp_X]/mL
  • DATURA STRAMONIUM 12 [hp_X]/mL
  • ANDROCTONUS AUSTRALIS VENOM 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.
  • 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: 08-28-2018 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.

Pts/stress Remedy Product Label Images

Pts/stress Remedy 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:

Kali Phosphoricum 3X, Ambra Grisea 6X, Cacao 6X, Phosphoricum Acidum 6X, Arnica Montana 6X, 12X, 30X, Calcarea Carbonica 8X, Cerebrum Suis 8X, Glandula Suprarenalis Suis 8X, Lithium Carbonicum 8X, Aconitum Napellus 8X, 30X, Argemone Mexicana 12X, Arsenicum Album 12X, Cicuta Virosa 12X, Hyoscyamus Niger 12X, Ignatia Tigrinum 12X, Natrum Muriaticum 12X, Tarentula Hispanica 12X, Stramonium 12X, 30X, 60X, Buthus Australis 6C.

Homeopathic Indications:

For the temporary relief of symptoms of stress such as terror, horror, post traumatic stress, fight or flight response, recurring nightmares, difficulty sleeping, difficulty concentrating, restlessness, and easy irritability.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of symptoms of stress such as terror, horror, post traumatic stress, fight or flight response, recurring nightmares, difficulty sleeping, difficulty concentrating, restlessness, and easy irritability.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

If pregnant or breastfeeding, ask a health 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 a cool, dry place.

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:

1-10 drops under the tongue, 2 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 43742-1322-1HOMEOPATHICPTS/STRESSREMEDY1 FL OZ (30 ml)

* Please review the disclaimer below.