NDC 43742-0744 Inflammation II

Asafoetida, Kalmia Latifolia, Causticum, Colchicum Autumnale, Ferrum Metallicum, Gnaphalium Polycephalum, Lithium Benzoicum, Mercurius Praecipitatus Ruber, Rhus Tox, Spiraea Ulmaria

NDC Product Code 43742-0744

NDC CODE: 43742-0744

Proprietary Name: Inflammation II 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: Asafoetida, Kalmia Latifolia, Causticum, Colchicum Autumnale, Ferrum Metallicum, Gnaphalium Polycephalum, Lithium Benzoicum, Mercurius Praecipitatus Ruber, Rhus Tox, Spiraea Ulmaria 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 an iron supplement used to treat or prevent low blood levels of iron (e.g., for anemia or during pregnancy). Iron is an important mineral that the body needs to produce red blood cells and keep you in good health.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-0744-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Inflammation II with NDC 43742-0744 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Inflammation II is asafoetida, kalmia latifolia, causticum, colchicum autumnale, ferrum metallicum, gnaphalium polycephalum, lithium benzoicum, mercurius praecipitatus ruber, rhus tox, spiraea ulmaria. 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.

Inflammation II 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.

  • ASAFETIDA 8 [hp_X]/mL
  • KALMIA LATIFOLIA LEAF 8 [hp_X]/mL
  • CAUSTICUM 10 [hp_X]/mL
  • COLCHICUM AUTUMNALE BULB 10 [hp_X]/mL
  • IRON 10 [hp_X]/mL
  • PSEUDOGNAPHALIUM OBTUSIFOLIUM 10 [hp_X]/mL
  • LITHIUM BENZOATE 10 [hp_X]/mL
  • MERCURIC OXIDE 10 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/mL
  • FILIPENDULA ULMARIA ROOT 10 [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: 05-04-2016 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: 06-18-2021 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.

Inflammation II Product Label Images

Inflammation II 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:

Asafoetida 8X, Kalmia Latifolia 8X, Causticum 10X, Colchicum Autumnale 10X, Ferrum Metallicum 10X, Gnaphalium Polycephalum 10X, Lithium Benzoicum 10X, Mercurius Praecipitatus Ruber, Rhus Tox 10X, Spiraea Ulmaria 10X.

Homeopathic Indications:

For temporary relief of pain, stiffness, inflammation, and conditions of the tendons and ligaments; backache, shoulder and arm pain, joint pain.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For temporary relief of pain, stiffness, inflammation, and conditions of the tendons and ligaments; backache, shoulder and arm pain, joint pain.****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 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 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 43742-0744-1HOMEOPATHICINFLAMMATION II1 FL OZ (30 ml)

* Please review the disclaimer below.