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  5. NDC Package Code: 50845-0109-2 Pms

NDC Package 50845-0109-2 Pms

Apis Mellifica,Chamomilla,Cimicifuga Racemosa,Cuprum Metallicum,Ignatia Amara,Kali - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
50845-0109-2
Package Description:
1 BOTTLE, SPRAY in 1 CARTON / 30 mL in 1 BOTTLE, SPRAY (50845-0109-1)
Product Code:
50845-0109
Proprietary Name:
Pms
Non-Proprietary Name:
Apis Mellifica, Chamomilla, Cimicifuga Racemosa, Cuprum Metallicum, Ignatia Amara, Kali Iodatum, Magnesia Phosphorica, Oophorinum (suis), Platinum Metallicum, Sepia, Thuja Occidentalis
Substance Name:
Apis Mellifera; Black Cohosh; Copper; Magnesium Phosphate, Dibasic Trihydrate; Matricaria Chamomilla Whole; Platinum; Potassium Iodide; Sepia Officinalis Juice; Strychnos Ignatii Seed; Sus Scrofa Ovary; Thuja Occidentalis Leafy Twig
Usage Information:
Adults and children over 12:  Spray twice under the tongue three times per day.  For severe symptoms, dosage may be taken up to six times the first day.Children 12 and under:  Consult a doctor prior to use.
11-Digit NDC Billing Format:
50845010902
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.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
07-18-2011
Listing Expiration Date:
12-31-2025
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 50845-0109-2?

The NDC Packaged Code 50845-0109-2 is assigned to a package of 1 bottle, spray in 1 carton / 30 ml in 1 bottle, spray (50845-0109-1) of Pms, 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 50845-0109 included in the NDC Directory?

Yes, Pms with product code 50845-0109 is active and included in the NDC Directory. The product was first marketed by Liddell Laboratories, Inc. on July 18, 2011 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 50845-0109-2?

The 11-digit format is 50845010902. 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
5-4-150845-0109-25-4-250845-0109-02