NDC 43742-0849 Inflammation II
Asafoetida,Kalmia Latifolia,Causticum,Colchicum Autumnale,Ferrum Metallicum,Gnaphalium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-0849 - Inflammation
Product Packages
NDC Code 43742-0849-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-0849?
What are the uses for Inflammation II?
What are Inflammation II Active Ingredients?
- CAUSTICUM 10 [hp_X]/mL
- COLCHICUM AUTUMNALE BULB 10 [hp_X]/mL
- FERULA ASSA-FOETIDA RESIN 8 [hp_X]/mL
- FILIPENDULA ULMARIA ROOT 10 [hp_X]/mL
- IRON 10 [hp_X]/mL - A metallic element with atomic symbol Fe, atomic number 26, and atomic weight 55.85. It is an essential constituent of HEMOGLOBINS; CYTOCHROMES; and IRON-BINDING PROTEINS. It plays a role in cellular redox reactions and in the transport of OXYGEN.
- KALMIA LATIFOLIA LEAF 8 [hp_X]/mL
- LITHIUM BENZOATE 10 [hp_X]/mL
- MERCURIC OXIDE 10 [hp_X]/mL
- PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE 10 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/mL
Which are Inflammation II UNII Codes?
The UNII codes for the active ingredients in this product are:
- FERULA ASSA-FOETIDA RESIN (UNII: W9FZA51AS1)
- ASAFETIDA (UNII: W9FZA51AS1) (Active Moiety)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
- PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW)
- PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW) (Active Moiety)
- LITHIUM BENZOATE (UNII: R9Z042Z19E)
- LITHIUM CATION (UNII: 8H8Z5UER66) (Active Moiety)
- MERCURIC OXIDE (UNII: IY191986AO)
- MERCURIC OXIDE (UNII: IY191986AO) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS)
- FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS) (Active Moiety)
Which are Inflammation II Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Inflammation II?
* Please review the disclaimer below.
[1] 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.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] 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.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".