NDC 43742-0325 Bio Lymphomyosot

NDC Product Code 43742-0325

NDC 43742-0325-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Bio Lymphomyosot with NDC 43742-0325 is a product labeled by Deseret Biologicals, Inc.. The generic name of Bio Lymphomyosot is . The product's dosage form is and is administered via form.

Labeler Name: Deseret Biologicals, Inc.

Dosage Form: -

Product Type: 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.

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)

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
Start Marketing Date: 08-29-2014 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: 12-31-2019 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: I 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’.

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Bio Lymphomyosot Product Label Images

Bio Lymphomyosot 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:

Myosotis Arvensis 3X, Scrophularia Nodosa 3X, Teucrium Scorodonia 3X, Veronica Officinalis 3X, Equisetum Hyemale 4X, Fumaria Officinalis 4X, Geranium Robertianum 4X, Nasturtium Aquaticum 4X, Natrum Sulphuricum 4X, Pinus Sylvestris 4X, Gentiana Lutea 5X, Juglans Regia 5X, Aranea Diadema 6X, Sarsaparilla (Smilax Regelii) 6X, Ascorbic Acid 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Quercetin 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Calcarea Phosphorica 12X, Ferrum Iodatum 12X, Thyroidinum (suis) 12X, Gaertner Bacillus 30X

Indications:

For the temporary relief of swelling due to poor circulation, minor injury, and environmental toxins.

For the temporary relief of swelling due to poor circulation, minor injury, and environmental toxins.

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, seek advice of 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, 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 Parkland DriveSandy, UT 84070 www.desbio.com

Package Label Display

DESBIONDC 43742-0325-1HOMEOPATHIC BIOLYMPHOMYOSOT1 FL OZ (30 ml)

* Please review the disclaimer below.