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  4. NDC Product Code: 43742-1018 Pre-dental Visit

NDC 43742-1018 Pre-dental Visit

Scrophularia Nodosa,Teucrium Scorodonia,Veronica Officinalis,Equisetum Arvense,Fumaria - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1018?
  4. Pre-dental Visit Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
43742-1018
Proprietary Name:
Pre-dental Visit
Non-Proprietary Name: [1]
Scrophularia Nodosa, Teucrium Scorodonia, Veronica Officinalis, Equisetum Arvense, Fumaria Officinalis, Geranium Robertianum, Nasturtium Aquaticum, Natrum Sulphuricum, Pinus Sylvestris, Gentiana Lutea, Juglans Regia, Sarsaparilla (smilax Regelii), Clematis Vitalba, Flos, Helianthemum Nummularium, Flos, Impatiens Glandulifera, Flos, Ornithogalum Umbellatum, Flos, Prunus Cerasifera, Flos, Myosotis Arvensis, Aranea Diadema, Calcarea Phosphorica, Ferrum Iodatum, Lymph Node (suis), Thyroidinum (suis)
Substance Name: [2]
Araneus Diadematus; Clematis Vitalba Flower; Equisetum Arvense Top; Ferrous Iodide; Fumaria Officinalis Flowering Top; Gentiana Lutea Root; Geranium Robertianum; Helianthemum Nummularium Flower; Impatiens Glandulifera Flower; Juglans Regia Fruit Rind, Immature; Juglans Regia Leaf; Myosotis Arvensis; Nasturtium Officinale; Ornithogalum Umbellatum Flowering Top; Pinus Sylvestris Leafy Twig; Prunus Cerasifera Flower; Sarsaparilla; Scrophularia Nodosa; Sodium Sulfate; Sus Scrofa Lymph; Sus Scrofa Thyroid; Teucrium Scorodonia Flowering Top; 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:
    4d3defe9-9f31-4678-8e33-3e54e3fd777b
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    01-16-2018
    End Marketing Date: [10]
    06-18-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 43742-1018?

    The NDC code 43742-1018 is assigned by the FDA to the product Pre-dental Visit which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Pre-dental Visit is scrophularia nodosa, teucrium scorodonia, veronica officinalis, equisetum arvense, fumaria officinalis, geranium robertianum, nasturtium aquaticum, natrum sulphuricum, pinus sylvestris, gentiana lutea, juglans regia, sarsaparilla (smilax regelii), clematis vitalba, flos, helianthemum nummularium, flos, impatiens glandulifera, flos, ornithogalum umbellatum, flos, prunus cerasifera, flos, myosotis arvensis, aranea diadema, 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 43742-1018-1 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 Pre-dental Visit?

    For the temporary relief of dental pain, soreness, tenderness and swelling prior to dental appointment.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration. For the temporary relief of dental pain, soreness, tenderness and swelling prior to dental appointment.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

    What are Pre-dental Visit 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 Pre-dental Visit UNII Codes?

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

    • SCROPHULARIA NODOSA (UNII: 7H443NUB2T)
    • SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (Active Moiety)
    • 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 ARVENSE TOP (UNII: 1DP6Y6B65Z)
    • EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (Active Moiety)
    • FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL)
    • FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL) (Active Moiety)
    • GERANIUM ROBERTIANUM (UNII: R5I1HK0UBL)
    • GERANIUM ROBERTIANUM (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)
    • JUGLANS REGIA FRUIT RIND, IMMATURE (UNII: ZPS7Q5U53K)
    • JUGLANS REGIA FRUIT RIND, IMMATURE (UNII: ZPS7Q5U53K) (Active Moiety)
    • JUGLANS REGIA LEAF (UNII: 85HKB87105)
    • JUGLANS REGIA LEAF (UNII: 85HKB87105) (Active Moiety)
    • SARSAPARILLA (UNII: 2H1576D5WG)
    • SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
    • CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI)
    • CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI) (Active Moiety)
    • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP)
    • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP) (Active Moiety)
    • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
    • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
    • ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B)
    • ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B) (Active Moiety)
    • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS)
    • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS) (Active Moiety)
    • MYOSOTIS ARVENSIS (UNII: C73BK97H5J)
    • MYOSOTIS ARVENSIS (UNII: C73BK97H5J) (Active Moiety)
    • ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5)
    • ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5) (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 Pre-dental Visit 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 Pre-dental Visit?

    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.

    [10] 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.

    [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".