NDC 43742-1620 Intimate

Natrum Carbonicum, Saccharum Officinale, Lithium Carbonicum, Placenta Totalis Suis, Lac Caninum, Anacardium Orientale, Aurum Muriaticum Natronatum, Camphora, Germanium Metallicum, Helleborus Niger, Magnesia Oxydata, Rhus Glabra, Stramonium, Thuja Occidentalis, Dna (human), Oxytocin, Hydrogen, Neon, Lac Materna Humanum

NDC Product Code 43742-1620

NDC CODE: 43742-1620

Proprietary Name: Intimate 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: Natrum Carbonicum, Saccharum Officinale, Lithium Carbonicum, Placenta Totalis Suis, Lac Caninum, Anacardium Orientale, Aurum Muriaticum Natronatum, Camphora, Germanium Metallicum, Helleborus Niger, Magnesia Oxydata, Rhus Glabra, Stramonium, Thuja Occidentalis, Dna (human), Oxytocin, Hydrogen, Neon, Lac Materna Humanum 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.
  • This medication is a mineral supplement used to prevent and treat low amounts of magnesium in the blood. Some brands are also used to treat symptoms of too much stomach acid such as stomach upset, heartburn, and acid indigestion. Magnesium is very important for the normal functioning of cells, nerves, muscles, bones, and the heart. Usually, a well-balanced diet provides normal blood levels of magnesium. However, certain situations cause your body to lose magnesium faster than you can replace it from your diet. These situations include treatment with water pills (diuretics such as furosemide, hydrochlorothiazide), a poor diet, alcoholism, or other medical conditions (e.g., severe diarrhea/vomiting, stomach/intestinal absorption problems, poorly controlled diabetes).
  • Drug uses not available

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-1620-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Intimate with NDC 43742-1620 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Intimate is natrum carbonicum, saccharum officinale, lithium carbonicum, placenta totalis suis, lac caninum, anacardium orientale, aurum muriaticum natronatum, camphora, germanium metallicum, helleborus niger, magnesia oxydata, rhus glabra, stramonium, thuja occidentalis, dna (human), oxytocin, hydrogen, neon, lac materna humanum. 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.

Intimate 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.

  • SODIUM CARBONATE 6 [hp_X]/mL
  • SUCROSE 6 [hp_X]/mL
  • LITHIUM CARBONATE 8 [hp_X]/mL
  • SUS SCROFA PLACENTA 8 [hp_X]/mL
  • CANIS LUPUS FAMILIARIS MILK 10 [hp_X]/mL
  • SEMECARPUS ANACARDIUM JUICE 12 [hp_X]/mL
  • SODIUM TETRACHLOROAURATE 12 [hp_X]/mL
  • CAMPHOR (NATURAL) 12 [hp_X]/mL
  • GERMANIUM SESQUIOXIDE 12 [hp_X]/mL
  • HELLEBORUS NIGER ROOT 12 [hp_X]/mL
  • MAGNESIUM OXIDE 12 [hp_X]/mL
  • RHUS GLABRA TOP 12 [hp_X]/mL
  • DATURA STRAMONIUM 12 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL
  • HERRING SPERM DNA 12 [hp_X]/mL
  • OXYTOCIN 12 [hp_X]/mL
  • HYDROGEN 16 [hp_X]/mL
  • NEON 16 [hp_X]/mL
  • HUMAN MILK 16 [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.
  • 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: 03-09-2020 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: 12-31-2021 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.

Intimate Product Label Images

Intimate 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:

Natrum Carbonicum 6X, Saccharum Officinale 6X, Lithium Carbonicum 8X, Placenta Totalis Suis 8X, 12X, 30X, 200X, Lac Caninum 10X, Anacardium Orientale 12X, Aurum Muriaticum Natronatum 12X, Camphora 12X, Germanium Metallicum 12X, Helleborus Niger 12X, Magnesia Oxydata 12X, Rhus Glabra 12X, Stramonium 12X, Thuja Occidentalis 12X, DNA (Human) 12X, 30X, 200X, Oxytocin 12X, 30X, 200X, Hydrogen 16X, Neon 16X, Lac Materna Humanum 16X, 30X, 200X.

Homeopathic Indications:

For the temporary relief of symptoms related to issues with intimacy, such as forsaken feelings, isolation, disconnection, lack of mother-child bond, alienation, loneliness, estranged, and feeling unloved.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of symptoms related to issues with intimacy, such as forsaken feelings, isolation, disconnection, lack of mother-child bond, alienation, loneliness, estranged, and feeling unloved.****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 84070 www.desbio.com

Package Label Display:

DESBIONDC 43742-1620-1HOMEOPATHICINTIMATE1 FL OZ (30 ml)

* Please review the disclaimer below.