NDC Package 50845-0266-1 Candida Yeast

Baptisia Tinctoria,Borax,Candida Albicans,Candida Parapsilosis,Cinchona - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
50845-0266-1
Package Description:
30 mL in 1 BOTTLE, SPRAY
Product Code:
Proprietary Name:
Candida Yeast
Non-Proprietary Name:
Baptisia Tinctoria, Borax, Candida Albicans, Candida Parapsilosis, Cinchona Officinalis, Echinacea (angustifolia), Nitricum Acidum, Pulsatilla (pratensis), Pyrogenium, Sepia, Sulphuricum Acidum, Thuja Occidentalis
Substance Name:
Anemone Pratensis; Baptisia Tinctoria Root; Candida Albicans; Candida Parapsilosis; Cinchona Officinalis Bark; Echinacea Angustifolia Whole; Nitric Acid; Rancid Beef; Sepia Officinalis Juice; Sodium Borate; Sulfuric Acid; Thuja Occidentalis Leafy Twig
Usage Information:
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.
11-Digit NDC Billing Format:
50845026601
Product Type:
Human Otc Drug
Labeler Name:
Liddell Laboratories, Inc.
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    03-18-2020
    End Marketing Date:
    03-26-2025
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50845-0266-1?

    The NDC Packaged Code 50845-0266-1 is assigned to a package of 30 ml in 1 bottle, spray of Candida Yeast, a human over the counter drug labeled by Liddell Laboratories, Inc.. The product's dosage form is spray and is administered via oral form.

    Is NDC 50845-0266 included in the NDC Directory?

    Yes, Candida Yeast with product code 50845-0266 is active and included in the NDC Directory. The product was first marketed by Liddell Laboratories, Inc. on March 18, 2020.

    What is the 11-digit format for NDC 50845-0266-1?

    The 11-digit format is 50845026601. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-150845-0266-15-4-250845-0266-01