NDC Package 43742-1320-1 Pertussis

Ipecacuanha,Sticta Pulmonaria,Phosphorus,Antimonium Tartaricum,Kreosotum,Aconitum - 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:
43742-1320-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Pertussis
Non-Proprietary Name:
Ipecacuanha, Sticta Pulmonaria, Phosphorus, Antimonium Tartaricum, Kreosotum, Aconitum Napellus, Bryonia (alba), Hyoscyamus Niger, Silicea, Tabacum, Pertussinum, Tetanus Toxin
Substance Name:
Aconitum Napellus; Antimony Potassium Tartrate; Bryonia Alba Root; Clostridium Tetani; Human Sputum, Bordetella Pertussis Infected; Hyoscyamus Niger; Ipecac; Lobaria Pulmonaria; Phosphorus; Silicon Dioxide; Tobacco Leaf; Wood Creosote
Usage Information:
For temporary relief of symptoms related to Pertussis infection including cough, bronchial congestion, fever, and vaccinationreactions.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to Pertussis infection including cough, bronchial congestion, fever, and vaccinationreactions.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742132001
Product Type:
Human Otc Drug
Labeler Name:
Deseret Biologicals, 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:
    09-04-2018
    End Marketing Date:
    05-13-2025
    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 43742-1320-1?

    The NDC Packaged Code 43742-1320-1 is assigned to a package of 30 ml in 1 bottle, dropper of Pertussis, a human over the counter drug labeled by Deseret Biologicals, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 43742-1320 included in the NDC Directory?

    Yes, Pertussis with product code 43742-1320 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on September 04, 2018.

    What is the 11-digit format for NDC 43742-1320-1?

    The 11-digit format is 43742132001. 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
    5-4-143742-1320-15-4-243742-1320-01