NDC Package 43742-1221-1 Rheumatism

Benzoicum Acidum,Rhododendron Chrysanthum,Spiraea Ulmaria,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:
43742-1221-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Rheumatism
Non-Proprietary Name:
Benzoicum Acidum, Rhododendron Chrysanthum, Spiraea Ulmaria, Aconitum Napellus, Dulcamara, Ledum Palustre, Pulsatilla (vulgaris), Asclepias Tuberosa, Lithium Benzoicum, Euphorbium Officinarum
Substance Name:
Aconitum Napellus; Anemone Pulsatilla; Asclepias Tuberosa Root; Benzoic Acid; Euphorbia Resinifera Resin; Filipendula Ulmaria Root; Lithium Benzoate; Rhododendron Aureum Leaf; Rhododendron Tomentosum Leafy Twig; Solanum Dulcamara Top
Usage Information:
For temporary relief of symptoms related to rheumatism including joint pain, fever, inflammation and pain of leg(s).****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to rheumatism including joint pain, fever, inflammation and pain of leg(s).****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742122101
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:
    05-29-2018
    End Marketing Date:
    11-21-2024
    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 43742-1221-1?

    The NDC Packaged Code 43742-1221-1 is assigned to a package of 30 ml in 1 bottle, dropper of Rheumatism, 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 43742-1221 included in the NDC Directory?

    Yes, Rheumatism with product code 43742-1221 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on May 29, 2018.

    What is the 11-digit format for NDC 43742-1221-1?

    The 11-digit format is 43742122101. 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
    5-4-143742-1221-15-4-243742-1221-01