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NDC 54973-4069 Prid

Ichthammol,Calcium Sulfide,Calendula Officinalis Flowering Top,Arnica Montana,Echinacea - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 54973-4069?
  5. Prid Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
54973-4069
Proprietary Name:
Prid
Non-Proprietary Name: [1]
Ichthammol, Calcium Sulfide, Calendula Officinalis Flowering Top, Arnica Montana, Echinacea Angustifolia, Silicon Dioxide, Sulfur
Substance Name: [2]
Arnica Montana; Calcium Sulfide; Calendula Officinalis Flowering Top; Echinacea Angustifolia; Ichthammol; Silicon Dioxide; Sulfur
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Salve - A thick ointment or cerate (a fat or wax based preparation with a consistency between an ointment and a plaster).
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Labeler Name: [5]
    Hyland's Inc.
    Labeler Code:
    54973
    Product Label ID:
    d22eca2f-d7e6-3412-e053-2995a90a6384
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    03-01-2022
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Characteristics

    Color(s):
    BROWN (C48332 - BROWN TO DARK BROWN)

    Code Structure Chart

    Product Details

    What is NDC 54973-4069?

    The NDC code 54973-4069 is assigned by the FDA to the product Prid which is a human over the counter drug product labeled by Hyland's Inc.. The generic name of Prid is ichthammol, calcium sulfide, calendula officinalis flowering top, arnica montana, echinacea angustifolia, silicon dioxide, sulfur. The product's dosage form is salve and is administered via topical form. The product is distributed in a single package with assigned NDC code 54973-4069-1 1 can in 1 carton / 18 g in 1 can. 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 Prid?

    This product is used as May help draw out splinters & ingrown hairs and temporarily relieve pain, itchiness and irritation from: boils, minor skin eruptions, bites superficial cuts or scratches. May help draw out splinters & ingrown hairs and temporarily relieve pain, itchiness and irritation from: ■ boils ■ minor skin eruptions ■ bites ■ superficial cuts or scratches

    What are Prid 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 Prid UNII Codes?

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

    Which are Prid 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".