NDC Package 43406-0672-1 Candida Hp

Baptisia Tinctoria Root,Echinacea Purpurea,Glycyrrhiza Glabra,Astragalus Nuttallii - 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:
43406-0672-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Candida Hp
Non-Proprietary Name:
Baptisia Tinctoria Root, Echinacea Purpurea, Glycyrrhiza Glabra, Astragalus Nuttallii Leaf, Candida Albicans, Sodium Borate, Oyster Shell Calcium Carbonate, Crude, Wood Creosote, Lycopodium Clavatum Spore, Strychnos Nux-vomica Seed, Phosphoric Acid, Anemone Pulsatilla, Sepia Officinalis Juice, Thuja Occidentalis Leafy Twig, Sodium Phosphate, Dibasic, Heptahydrate, Nitric Acid
Substance Name:
Astragalus Nuttallii Leaf; Baptisia Tinctoria Root; Candida Albicans; Echinacea Purpurea; Glycyrrhiza Glabra; Lycopodium Clavatum Spore; Nitric Acid; Oyster Shell Calcium Carbonate, Crude; Phosphoric Acid; Pulsatilla Vulgaris; Sepia Officinalis Juice; Sodium Borate; Sodium Phosphate, Dibasic, Heptahydrate; Strychnos Nux-vomica Seed; Thuja Occidentalis Leafy Twig; Wood Creosote
Usage Information:
USES: Temporarily relieves symptoms associated with vaginal yeast infection.**
11-Digit NDC Billing Format:
43406067201
Product Type:
Human Otc Drug
Labeler Name:
Natural Creations, 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:
    01-01-2018
    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 43406-0672-1?

    The NDC Packaged Code 43406-0672-1 is assigned to a package of 30 ml in 1 bottle, dropper of Candida Hp, a human over the counter drug labeled by Natural Creations, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 43406-0672 included in the NDC Directory?

    Yes, Candida Hp with product code 43406-0672 is active and included in the NDC Directory. The product was first marketed by Natural Creations, Inc. on January 01, 2018 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 43406-0672-1?

    The 11-digit format is 43406067201. 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
    5-4-143406-0672-15-4-243406-0672-01