NDC 43742-0153 Bacteria

NDC Product Code 43742-0153

NDC 43742-0153-1

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

Bacteria with NDC 43742-0153 is a product labeled by Deseret Biologicals, Inc. The generic name of Bacteria 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: 09-17-2012 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’.

* Please review the disclaimer below.

Bacteria Product Label Images

Bacteria 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:

Cochlearia armoracia 3X, Echinacea 3X, Hydrastis canadensis 3X, Lomatium dissectum 3X, Tabebuia impetiginosa 3X, Adrenalinum 8X, Hepar suis 8X, Lymph (suis) 8X, Spleen (suis) 8X, Thymus (suis) 8X, Thyroidinum (suis) 8X, Arnica montana 12X, Belladonna 12X, Ferrum metallicum 12X, Hypericum perforatum 12X, Iridium metallicum 12X, Nitricum acidum 12X, Nux vomica 12X, Phosphoricum acidum 12X, Phosphorus 12X, Selenium metallicum 12X, Zincum metallicum 12X.

Indications:

For temporary relief of symptoms related to bacterial infection including fever, headache, mucous congestion, stomach discomfort, cough and diarrhea.

For temporary relief of symptoms related to bacterial infection including fever, headache, mucous congestion, stomach discomfort, cough and diarrhea.

Warnings:

Keep out of reach of children. In case of overdose, contact 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.

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.

Keep Out Of Reach Of Children.

In case of overdose, contact physician or Poison Control Center right away.

Questions:

Dist. By:Deseret Biologicals, Inc.469 Parkland DriveSandy, UT 84070www.desbio.com

Package Label

DESBIONDC 43742-0153-1HOMEOPATHICBACTERIA1 FL OZ (30 ml)

* Please review the disclaimer below.