NDC 52747-255 Hylafem Boricum Acidum 3x

Boricum Acidum Suppository Vaginal - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
52747-255
Proprietary Name:
Hylafem Boricum Acidum 3x
Non-Proprietary Name: [1]
Boricum Acidum
Substance Name: [2]
Boric Acid
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Suppository - A solid body of various weights and shapes, adapted for introduction into the rectal orifice of the human body; they usually melt, soften, or dissolve at body temperature.
Administration Route(s): [4]
  • Vaginal - Administration into the vagina.
  • Labeler Name: [5]
    U.s. Pharmaceutical Corporation
    Labeler Code:
    52747
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    12-09-2019
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 52747-255-03

    Package Description: 1 CAPSULE in 1 CARTON / 3 SUPPOSITORY in 1 CAPSULE

    Product Details

    What is NDC 52747-255?

    The NDC code 52747-255 is assigned by the FDA to the product Hylafem Boricum Acidum 3x which is a human over the counter drug product labeled by U.s. Pharmaceutical Corporation. The generic name of Hylafem Boricum Acidum 3x is boricum acidum. The product's dosage form is suppository and is administered via vaginal form. The product is distributed in a single package with assigned NDC code 52747-255-03 1 capsule in 1 carton / 3 suppository in 1 capsule. 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 Hylafem Boricum Acidum 3x?

    This product is used as Boricum Acidum 3X* HPUS**                               Restores vaginal pH and relieves                                                                                vaginal itching, burning and irritation.*X is a homeopathic dilution. **The letters HPUS indicates that this ingredient is officially monographed in the Homeopathic Pharmacopoeia of the United States..  treats and relieves symptoms of vaginal and urinary infections rebalances vaginal pH and restores normal vaginal health helps relieve symptoms of external and internal vaginal burning, itching, irritation and dryness helps reduce vaginal odor due to vaginal infections

    What are Hylafem Boricum Acidum 3x 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 Hylafem Boricum Acidum 3x UNII Codes?

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

    Which are Hylafem Boricum Acidum 3x 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".