NDC 43742-0038 Lym

NDC Product Code 43742-0038

NDC 43742-0038-1

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

Lym with NDC 43742-0038 is a product labeled by Deseret Biologicals, Inc.. The generic name of Lym 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.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

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: 05-17-2012 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.

Lym Product Label Images

Lym 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

Otc - Active Ingredient

ACTIVE INGREDIENTS:  Arnica montana 3X, Calendula officinalis 3X, Echinacea 3X, Hydrastis canadensis 3X, Myrrha 3X, Phytolacca decandra 3X, Taraxacum officinale 3X, Trifolium pratense 3X, Trigonella foenum-graecum 3X, Urtica dioica 3X, Propolis 6X, Adrenalinum 8X, Gunpowder 8X, Thymus (suis) 8X, Thyroidinum (suis) 8X, Arsenicum album 12X, Cocculus indicus 12X, Iridium metallicum 12X, Lycopodium clavatum 12X, Phosphorus 12X, Rhus toxicodendron 12X, Borrelia burgdorferi 15X, 30X, 60X, 100X, 200X, Encephalitis virus 15X, 30X, 60X, 100X, 200X, Ledum palustre 30X, Meningococcus 30X, 60X, 100X, 200X, Hepatitis virus type B 33X, 60X, 100X, 200X.

Otc - Purpose

INDICATIONS:  For temporary relief of symptoms related to Lyme Disease including joint pain, severe headache, fever(s), severe muscle aches/pain, flu-like feelings of headache, stiff neck, fever, muscle aches, and profound fatigue, circular rash surrounding the site of a tick bite, vision changes and change in smell/taste; difficulty chewing, swallowing, or speaking; hoarseness or vocal cord problems; facial paralysis.

Warnings

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.

Dosage & Administration

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 Ingredient

INACTIVE INGREDIENTS:  Demineralized water, 25% Ethanol.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.  In case of overdose, contact physician or Poison Control Center right away.

Indications & Usage

INDICATIONS:  For temporary relief of symptoms related to Lyme Disease including joint pain, severe headache, fever(s), severe muscle aches/pain, flu-like feelings of headache, stiff neck, fever, muscle aches, and profound fatigue, circular rash surrounding the site of a tick bite, vision changes and change in smell/taste; difficulty chewing, swallowing, or speaking; hoarseness or vocal cord problems, facial paralysis.

Otc - Questions

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

* Please review the disclaimer below.