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NDC 68093-0668 Yeast Gard Advanced

Berberis Vulgaris,Borax,Collinsonia Canadensis,Hamamelis Virginiana Douche Vaginal - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 68093-0668?
  4. Yeast Gard Advanced Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
68093-0668
Proprietary Name:
Yeast Gard Advanced
Non-Proprietary Name: [1]
Berberis Vulgaris, Borax, Collinsonia Canadensis, Hamamelis Virginiana
Substance Name: [2]
Berberis Vulgaris Root Bark; Collinsonia Canadensis Root; Hamamelis Virginiana Root Bark/stem Bark; Sodium Borate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Douche - A liquid preparation, intended for the irrigative cleansing of the vagina, that is prepared from powders, liquid solutions, or liquid concentrates and contains one or more chemical substances dissolved in a suitable solvent or mutually miscible solvents.
Administration Route(s): [4]
  • Vaginal - Administration into the vagina.
    • Labeler Name: [5]
    Wisconsin Pharmacal Company
    Labeler Code:
    68093
    Product Label ID:
    0dfe58cd-713c-4a0d-88e2-1604fe13292a
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    10-01-2007
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 68093-0668?

    The NDC code 68093-0668 is assigned by the FDA to the product Yeast Gard Advanced which is a human over the counter drug product labeled by Wisconsin Pharmacal Company. The generic name of Yeast Gard Advanced is berberis vulgaris, borax, collinsonia canadensis, hamamelis virginiana. The product's dosage form is douche and is administered via vaginal form. The product is distributed in a single package with assigned NDC code 68093-0668-1 2 bottle in 1 carton / 133.07 g in 1 bottle. 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 Yeast Gard Advanced?

    DirectionsTamper Evident: If the foil seal on bottle opening is missing, torn or damaged in any way, do not use.Wash hands thoroughly with soap and water before and after useremove cap and safety seal from bottle. Carefully open teh packet and pour homeopathic contents into the douche bottle. Screw cap back onto bottle and shake thoroughly to fully mix powder into solution. After fully mixed, remove cap. Remove sanitary wrap from nozzle. Screw nozzle onto douche bottle.Slowly insert nozzle into vagina about 3 inches. If needed, a small amount of personal lubricant can be applied to nozzle to ease insertion of nozzle into vagina. Gently squeeze bottle until solution is dispensed. Use while sittion on the toilet, standing in the shower or in the tub. After douching discard bottle and nozzle.

    What are Yeast Gard Advanced 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 Yeast Gard Advanced UNII Codes?

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

    • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
    • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
    • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
    • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
    • SODIUM BORATE (UNII: 91MBZ8H3QO)
    • BORATE ION (UNII: 44OAE30D22) (Active Moiety)
    • COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR)
    • COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (Active Moiety)

    Which are Yeast Gard Advanced 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".