NDC 50845-0266 Candida Yeast

Baptisia Tinctoria, Borax, Candida Albicans, Candida Parapsilosis, Cinchona Officinalis, Echinacea (angustifolia), Nitricum Acidum, Pulsatilla (pratensis), Pyrogenium, Sepia, Sulphuricum Acidum, Thuja Occidentalis

NDC Product Code 50845-0266

NDC CODE: 50845-0266

Proprietary Name: Candida Yeast What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Baptisia Tinctoria, Borax, Candida Albicans, Candida Parapsilosis, Cinchona Officinalis, Echinacea (angustifolia), Nitricum Acidum, Pulsatilla (pratensis), Pyrogenium, Sepia, Sulphuricum Acidum, Thuja Occidentalis 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.

NDC Code Structure

  • 50845 - Liddell Laboratories, Inc.

NDC 50845-0266-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

NDC Product Information

Candida Yeast with NDC 50845-0266 is a a human over the counter drug product labeled by Liddell Laboratories, Inc.. The generic name of Candida Yeast is baptisia tinctoria, borax, candida albicans, candida parapsilosis, cinchona officinalis, echinacea (angustifolia), nitricum acidum, pulsatilla (pratensis), pyrogenium, sepia, sulphuricum acidum, thuja occidentalis. The product's dosage form is spray and is administered via oral form.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug 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.

Candida Yeast Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Liddell Laboratories, Inc.
Labeler Code: 50845
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 03-18-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Candida Yeast Product Label Images

Candida Yeast Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

(in each spray) 8.33% of Baptisia Tinctoria 3X, Borax 30C, Candida Albicans 12X, Candida Parapsilosis 8C, Cinchona Officinalis 30C, Echinacea (Angustifolia) 3X, Nitricum Acidum 30C, Pulsatilla (Pratensis) 30C, Pyrogenium 200C, Sepia 30C, Sulphuricum Acidum 30C, Thuja Occidentalis 30C.

Indications:

May temporarily relieve symptoms of Candida infections: vaginal discharge, vaginal discomfort, abdominal distention, bloating.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

May temporarily relieve symptoms of Candida infections: vaginal discharge, vaginal discomfort, abdominal distention, bloating.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings:

If symptoms persist for more than 7 days, consult a doctor.If pregnant or breast feeding, ask a doctor before use.Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

Keep Out Of Reach Of Children.

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

Directions:

Adults and children over 12: Spray twice under the tongue 3 times per day.Children 12 and under: Consult a doctor prior to use.

Inactive Ingredients:

Organic alcohol 20% v/v, Purified water.

Questions:

DIST. BY LIDDELL LABORATORIES, INC.WOODBINE, IA 51579WWW.LIDDELL.NET 1-800-460-7733

Package Label Display:

ORAL SPRAYSLIDDELLLABORATORIES21CanCandida YeastHOMEOPATHIC1.0 fl. oz. (30 ml)

* Please review the disclaimer below.