NDC 43742-1182 Lymph/spleen Combo

Juniperus Communis, Phytolacca Decandra, Quercus Glandium Spiritus, Myosotis Arvensis, Natrum Sulphuricum, Ceanothus Americanus, Helianthus Annuus, Natrum Muriaticum, Lymph Node (suis), Spleen (suis), Thymus (suis), Chininum Arsenicosum, Castanea Vesca, Adenosinum Triphosphoricum Dinatrum, Ubidecarenonum, Ferrum Metallicum, Succinum, Apis Mellifica

NDC Product Code 43742-1182

NDC Code: 43742-1182

Proprietary Name: Lymph/spleen Combo 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: Juniperus Communis, Phytolacca Decandra, Quercus Glandium Spiritus, Myosotis Arvensis, Natrum Sulphuricum, Ceanothus Americanus, Helianthus Annuus, Natrum Muriaticum, Lymph Node (suis), Spleen (suis), Thymus (suis), Chininum Arsenicosum, Castanea Vesca, Adenosinum Triphosphoricum Dinatrum, Ubidecarenonum, Ferrum Metallicum, Succinum, Apis Mellifica 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.
    • 43742-1182 - Lymph/spleen Combo

NDC 43742-1182-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Lymph/spleen Combo with NDC 43742-1182 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Lymph/spleen Combo is juniperus communis, phytolacca decandra, quercus glandium spiritus, myosotis arvensis, natrum sulphuricum, ceanothus americanus, helianthus annuus, natrum muriaticum, lymph node (suis), spleen (suis), thymus (suis), chininum arsenicosum, castanea vesca, adenosinum triphosphoricum dinatrum, ubidecarenonum, ferrum metallicum, succinum, apis mellifica. 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.

Lymph/spleen Combo 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.

  • JUNIPERUS COMMUNIS WHOLE 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
  • QUERCUS ROBUR NUT 4 [hp_X]/mL
  • MYOSOTIS ARVENSIS 6 [hp_X]/mL
  • SODIUM SULFATE 6 [hp_X]/mL
  • CEANOTHUS AMERICANUS LEAF 6 [hp_X]/mL
  • HELIANTHUS ANNUUS FLOWERING TOP 6 [hp_X]/mL
  • SODIUM CHLORIDE 6 [hp_X]/mL
  • SUS SCROFA LYMPH 8 [hp_X]/mL
  • SUS SCROFA SPLEEN 8 [hp_X]/mL
  • SUS SCROFA THYMUS 8 [hp_X]/mL
  • QUININE ARSENATE 8 [hp_X]/mL
  • CASTANEA SATIVA LEAF 9 [hp_X]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 12 [hp_X]/mL
  • UBIDECARENONE 12 [hp_X]/mL
  • IRON 30 [hp_X]/mL
  • AMBER 30 [hp_X]/mL
  • APIS MELLIFERA 200 [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: 02-27-2018 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 07-18-2023 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.

Lymph/spleen Combo Product Label Images

Lymph/spleen Combo 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:

Juniperus Communis 3X, Phytolacca Decandra 4X, Quercus Glandium Spiritus 4X, Myosotis Arvensis 6X, 12X, Natrum Sulphuricum 6X, 12X, Ceanothus Americanus 6X, 12X, 30X, 200C, Helianthus Annuus 6X, 12X, 30X, 200C, Natrum Muriaticum 6X, 12X, 30X, 200C, Lymph Node (Suis) 8X, 12X, Spleen (Suis) 8X, 12X, Thymus (Suis) 8X, 12X, Chininum Arsenicosum 8X, 12X, 30C, Castanea Vesca 9X, Adenosinum Triphosphoricum Dinatrum 12X, 30X, Coenzyme Q10 12X, 30X, Ferrum Metallicum 30X, Succinum 30X, Apis Mellifica 200C.

Homeopathic Indications:

For temporary relief of symptoms related to lymphatic and spleen malfunction including lack of energy, lethargy, weakness and poor muscle tone, poor appetite and sense of taste, poor digestion, loose and watery stools, and poor concentration.****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 lymphatic and spleen malfunction including lack of energy, lethargy, weakness and poor muscle tone, poor appetite and sense of taste, poor digestion, loose and watery stools, and poor concentration.****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 43742-1182-1HOMEOPATHICLYMPH/SPLEENCOMBO1 FL OZ (30 ml)

* Please review the disclaimer below.

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