NDC Package 61657-0006-1 Anxiolix

Arsenicum Album , Scutellaria Lateriflora, Phosphorus, Lachesis Mutus, Pulsatilla, - 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:
61657-0006-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Anxiolix
Non-Proprietary Name:
Arsenicum Album , Scutellaria Lateriflora, Phosphorus, Lachesis Mutus, Pulsatilla, Passiflora Incarnata, Aconite, Valeriana Officinalis, Calcarea Carbonica, Ignatia Amara
Substance Name:
Aconitum Napellus; Arsenic Trioxide; Lachesis Muta Venom; Oyster Shell Calcium Carbonate, Crude; Passiflora Incarnata Flowering Top; Phosphorus; Pulsatilla Vulgaris; Scutellaria Lateriflora; Strychnos Ignatii Seed; Valerian
Usage Information:
INDICATIONS: FOR THE TEMPORARY RELIEF OF ANXIETY, SLEEPLESSNESS, NERVOUSNESS
11-Digit NDC Billing Format:
61657000601
Product Type:
Human Otc Drug
Labeler Name:
White Manufacturing Inc. Dba Micro West
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:
    06-01-2011
    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 61657-0006-1?

    The NDC Packaged Code 61657-0006-1 is assigned to a package of 30 ml in 1 bottle, dropper of Anxiolix, a human over the counter drug labeled by White Manufacturing Inc. Dba Micro West. The product's dosage form is liquid and is administered via oral form.

    Is NDC 61657-0006 included in the NDC Directory?

    Yes, Anxiolix with product code 61657-0006 is active and included in the NDC Directory. The product was first marketed by White Manufacturing Inc. Dba Micro West on June 01, 2011 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 61657-0006-1?

    The 11-digit format is 61657000601. 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
    5-4-161657-0006-15-4-261657-0006-01