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  4. NDC Product Code: 43742-1648 Sore Throat

NDC 43742-1648 Sore Throat

Teucrium Scorodonia,Veronica Officinalis,Equisetum Hyemale,Fumaria Officinalis,Geranium - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1648?
  4. Sore Throat Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
43742-1648
Proprietary Name:
Sore Throat
Non-Proprietary Name: [1]
Teucrium Scorodonia, Veronica Officinalis, Equisetum Hyemale, Fumaria Officinalis, Geranium Robertianum, Nasturtium Aquaticum, Natrum Sulphuricum, Pinus Sylvestris, Gentiana Lutea, Sarsaparilla (smilax Regelii), Scrophularia Nodosa, Myosotis Arvensis, Aranea Diadema, Juglans Regia, Calcarea Phosphorica, Ferrum Iodatum, Lymph Node (suis), Thyroidinum (suis)
Substance Name: [2]
Araneus Diadematus; Equisetum Hyemale Whole; Ferrous Iodide; Fumaria Officinalis Flowering Top; Gentiana Lutea Root; Geranium Robertianum Whole; Juglans Regia Fruit Rind, Immature; Juglans Regia Leaf; Myosotis Arvensis Whole; Nasturtium Officinale; Pinus Sylvestris Leafy Twig; Scrophularia Nodosa Whole; Smilax Ornata Root; Sodium Sulfate; Sus Scrofa Lymph; Teucrium Scorodonia Flowering Top; Thyroid; Tribasic Calcium Phosphate; Veronica Officinalis Flowering Top
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
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.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Deseret Biologicals, Inc.
    Labeler Code:
    43742
    Product Label ID:
    3d09dd25-5310-4ed5-9512-a160531425f3
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    05-27-2020
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 43742-1648?

    The NDC code 43742-1648 is assigned by the FDA to the product Sore Throat which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Sore Throat is teucrium scorodonia, veronica officinalis, equisetum hyemale, fumaria officinalis, geranium robertianum, nasturtium aquaticum, natrum sulphuricum, pinus sylvestris, gentiana lutea, sarsaparilla (smilax regelii), scrophularia nodosa, myosotis arvensis, aranea diadema, juglans regia, calcarea phosphorica, ferrum iodatum, lymph node (suis), thyroidinum (suis). The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 43742-1648-1 30 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Sore Throat?

    For temporary relief of symptoms related to both bacterial and viral throat infection including cough, sneezing, and pain.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to both bacterial and viral throat infection including cough, sneezing, and pain.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

    What are Sore Throat Active Ingredients?

    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.

    Which are Sore Throat UNII Codes?

    The UNII codes for the active ingredients in this product are:

    • TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G)
    • TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G) (Active Moiety)
    • VERONICA OFFICINALIS FLOWERING TOP (UNII: 9IH82J936J)
    • VERONICA OFFICINALIS FLOWERING TOP (UNII: 9IH82J936J) (Active Moiety)
    • EQUISETUM HYEMALE WHOLE (UNII: 59677RXH25)
    • EQUISETUM HYEMALE WHOLE (UNII: 59677RXH25) (Active Moiety)
    • FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL)
    • FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL) (Active Moiety)
    • GERANIUM ROBERTIANUM WHOLE (UNII: R5I1HK0UBL)
    • GERANIUM ROBERTIANUM WHOLE (UNII: R5I1HK0UBL) (Active Moiety)
    • NASTURTIUM OFFICINALE (UNII: YH89GMV676)
    • NASTURTIUM OFFICINALE (UNII: YH89GMV676) (Active Moiety)
    • SODIUM SULFATE (UNII: 0YPR65R21J)
    • SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
    • PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73)
    • PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73) (Active Moiety)
    • GENTIANA LUTEA ROOT (UNII: S72O3284MS)
    • GENTIANA LUTEA ROOT (UNII: S72O3284MS) (Active Moiety)
    • SMILAX ORNATA ROOT (UNII: 2H1576D5WG)
    • SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
    • SCROPHULARIA NODOSA WHOLE (UNII: 7H443NUB2T)
    • SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (Active Moiety)
    • MYOSOTIS ARVENSIS WHOLE (UNII: C73BK97H5J)
    • MYOSOTIS ARVENSIS WHOLE (UNII: C73BK97H5J) (Active Moiety)
    • ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5)
    • ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5) (Active Moiety)
    • JUGLANS REGIA LEAF (UNII: 85HKB87105)
    • JUGLANS REGIA LEAF (UNII: 85HKB87105) (Active Moiety)
    • JUGLANS REGIA FRUIT RIND, IMMATURE (UNII: ZPS7Q5U53K)
    • JUGLANS REGIA FRUIT RIND, IMMATURE (UNII: ZPS7Q5U53K) (Active Moiety)
    • TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
    • CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
    • FERROUS IODIDE (UNII: F5452U54PN)
    • FERROUS IODIDE (UNII: F5452U54PN) (Active Moiety)
    • SUS SCROFA LYMPH (UNII: 33A7VYU29L)
    • SUS SCROFA LYMPH (UNII: 33A7VYU29L) (Active Moiety)
    • SUS SCROFA THYROID (UNII: 6RV024OAUQ)
    • SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)

    Which are Sore Throat 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:

    Which are the Pharmacologic Classes for Sore Throat?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * Please review the disclaimer below.

    Product Footnotes

    [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".