NDC 62106-0630 Hptp

Arnica Montana,Achillea Millefolium,Erigeron Canadensis,Hydrastis Canadensis,Oryctolagus - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
62106-0630
Proprietary Name:
Hptp
Non-Proprietary Name: [1]
Arnica Montana, Achillea Millefolium, Erigeron Canadensis, Hydrastis Canadensis, Oryctolagus Cuniculus, Sabina, Secale Cornutum
Substance Name: [2]
Achillea Millefolium; Arnica Montana Root; Claviceps Purpurea Sclerotium; Conyza Canadensis; Goldenseal; Juniperus Sabina Leafy Twig; Oryctolagus Cuniculus Adrenal Gland; Oryctolagus Cuniculus Pituitary Gland
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]
  • Sublingual - Administration beneath the tongue.
  • Labeler Name: [5]
    Seroyal Usa
    Labeler Code:
    62106
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    10-26-2015
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 62106-0630-0

    Package Description: 1 BOTTLE, GLASS in 1 CARTON / 30 mL in 1 BOTTLE, GLASS

    Product Details

    What is NDC 62106-0630?

    The NDC code 62106-0630 is assigned by the FDA to the product Hptp which is a human over the counter drug product labeled by Seroyal Usa. The generic name of Hptp is arnica montana, achillea millefolium, erigeron canadensis, hydrastis canadensis, oryctolagus cuniculus, sabina, secale cornutum. The product's dosage form is liquid and is administered via sublingual form. The product is distributed in a single package with assigned NDC code 62106-0630-0 1 bottle, glass in 1 carton / 30 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 Hptp?

    UsesHelps promote and maintain growth and development normal energy levels.DirectionsTo be taken 20 minutes away from food.Place drops directly under the tongue or into ¼ oz of water.Adults and adolescents (12 years and older): Take 10 drops two to three times daily or as recommended by your healthcare practitioner. Children (under 12 years): Take under the direction of your healthcare practitioner.

    What are Hptp 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 Hptp UNII Codes?

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

    • JUNIPERUS SABINA LEAFY TWIG (UNII: Z5BEX9K2G1)
    • JUNIPERUS SABINA LEAFY TWIG (UNII: Z5BEX9K2G1) (Active Moiety)
    • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
    • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
    • ARNICA MONTANA ROOT (UNII: MUE8Y11327)
    • ARNICA MONTANA ROOT (UNII: MUE8Y11327) (Active Moiety)
    • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
    • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
    • CONYZA CANADENSIS (UNII: 16D08B0B9N)
    • CONYZA CANADENSIS (UNII: 16D08B0B9N) (Active Moiety)
    • GOLDENSEAL (UNII: ZW3Z11D0JV)
    • GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
    • ORYCTOLAGUS CUNICULUS PITUITARY GLAND (UNII: T9F9ZW799A)
    • ORYCTOLAGUS CUNICULUS PITUITARY GLAND (UNII: T9F9ZW799A) (Active Moiety)
    • ORYCTOLAGUS CUNICULUS ADRENAL GLAND (UNII: QGY289M89Q)
    • ORYCTOLAGUS CUNICULUS ADRENAL GLAND (UNII: QGY289M89Q) (Active Moiety)

    Which are Hptp 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:

    * 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".