NDC Package 57955-3017-8 Candida

Abies Canadensis,Agaricus Musc,Allium Cepa,Allium Sativum,Aloe,Antimonium - 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:
57955-3017-8
Package Description:
236 mL in 1 BOTTLE, SPRAY
Product Code:
Proprietary Name:
Candida
Non-Proprietary Name:
Abies Canadensis, Agaricus Musc, Allium Cepa, Allium Sativum, Aloe, Antimonium Crudum, Asafoetida, Borax, Candida Albicans, Candida Parapsilosis, Carpinus Betulus, Flos, Ignatia Amara, Lachesis Mutus, Lycopodium Clavatum, Malus Pumila, Flos, Olea Europaea, Flos, Phosphoricum Acidum, Phytolacca Decandra, Pulsatilla, Sabadilla, Sticta Pulmonaria, Sulphur, Thuja Occidentalis.
Substance Name:
Aloe; Amanita Muscaria Fruiting Body; Antimony Trisulfide; Candida Albicans; Candida Parapsilosis; Carpinus Betulus Flowering Top; Ferula Assa-foetida Resin; Garlic; Lachesis Muta Venom; Lobaria Pulmonaria; Lycopodium Clavatum Spore; Malus Domestica Flower; Olea Europaea Flower; Onion; Phosphoric Acid; Phytolacca Americana Root; Pulsatilla Patens Whole; Schoenocaulon Officinale Seed; Sodium Borate; Strychnos Ignatii Seed; Sulfur; Thuja Occidentalis Leafy Twig; Tsuga Canadensis Bark
Usage Information:
  Adults                                              1 teaspoon Children 6 - 12 years                      1/2 teaspoon Children under 6 years old           Consult a physician 2 times daily on an empty stomach, before breakfast and at bedtime.Reference image: Candida.jpg
11-Digit NDC Billing Format:
57955301708
Product Type:
Human Otc Drug
Labeler Name:
King Bio Inc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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:
    02-01-2022
    Listing Expiration Date:
    12-31-2024
    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 57955-3017-8?

    The NDC Packaged Code 57955-3017-8 is assigned to a package of 236 ml in 1 bottle, spray of Candida, a human over the counter drug labeled by King Bio Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 57955-3017 included in the NDC Directory?

    Yes, Candida with product code 57955-3017 is active and included in the NDC Directory. The product was first marketed by King Bio Inc. on February 01, 2022 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 57955-3017-8?

    The 11-digit format is 57955301708. 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
    5-4-157955-3017-85-4-257955-3017-08