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NDC 62106-1172 Unda 710

Apis Mellifica,Calendula Officinalis,Lycopodium Clavatum,Dulcamara,Aurum Metallicum Liquid - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62106-1172?
  4. Unda 710 Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
62106-1172
Proprietary Name:
Unda 710
Non-Proprietary Name: [1]
Apis Mellifica, Calendula Officinalis, Lycopodium Clavatum, Dulcamara, Aurum Metallicum
Substance Name: [2]
Apis Mellifera; Calendula Officinalis Flowering Top; Gold; Lycopodium Clavatum Spore; Solanum Dulcamara 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]
    Seroyal Usa
    Labeler Code:
    62106
    Product Label ID:
    1f64baba-eb29-30c6-e054-00144ff8d46c
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    09-10-2015
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 62106-1172-8

    Package Description: 1 BOTTLE, GLASS in 1 CARTON / 20 mL in 1 BOTTLE, GLASS

    Product Details

    What is NDC 62106-1172?

    The NDC code 62106-1172 is assigned by the FDA to the product Unda 710 which is a human over the counter drug product labeled by Seroyal Usa. The generic name of Unda 710 is apis mellifica, calendula officinalis, lycopodium clavatum, dulcamara, aurum metallicum. 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 62106-1172-8 1 bottle, glass in 1 carton / 20 ml in 1 bottle, glass. 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 Unda 710?

    Uses For the temporary relief of symptoms associated with cough. DirectionsAdults and adolescents (12 years and older): Take 5 drops three times daily or as recommended by your healthcare practitioner. Children (under 12 years): Take under the direction of your healthcare practitioner. Uses For the temporary relief of symptoms associated with common colds. DirectionsAdults and adolescents (12 years and older): Take 5 drops three times daily or as recommended by your healthcare practitioner. Children (under 12 years): Take under the direction of your healthcare practitioner.

    What are Unda 710 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 Unda 710 UNII Codes?

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

    • GOLD (UNII: 79Y1949PYO)
    • GOLD (UNII: 79Y1949PYO) (Active Moiety)
    • CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE)
    • CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE) (Active Moiety)
    • CRATAEGUS FRUIT (UNII: Q21UUL2105)
    • CRATAEGUS FRUIT (UNII: Q21UUL2105) (Active Moiety)
    • GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI)
    • GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI) (Active Moiety)
    • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
    • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
    • MENTHA PIPERITA (UNII: 79M2M2UDA9)
    • MENTHA PIPERITA (UNII: 79M2M2UDA9) (Active Moiety)
    • MYRTUS COMMUNIS TOP (UNII: 367E55FXGW)
    • MYRTUS COMMUNIS TOP (UNII: 367E55FXGW) (Active Moiety)
    • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
    • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
    • SOLANUM DULCAMARA TOP (UNII: KPS1B1162N)
    • SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (Active Moiety)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
    • APIS MELLIFERA (UNII: 7S82P3R43Z)
    • APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)

    Which are Unda 710 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 Unda 710?

    * 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".