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  5. NDC Package Code: 43742-1303-1 Inflammation

NDC Package 43742-1303-1 Inflammation

Arnica Montana,Benzoicum Acidum,Echinacea (angustifolia),Apis Mellifica,Baptisia - 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:
43742-1303-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43742-1303
Proprietary Name:
Inflammation
Non-Proprietary Name:
Arnica Montana, Benzoicum Acidum, Echinacea (angustifolia), Apis Mellifica, Baptisia Tinctoria, Dulcamara, Eucalyptus Globulus, Solanum Nigrum, Eupatorium Perfoliatum, Bryonia (alba), Colchicum Autumnale, Mercurialis Perennis, Rhus Tox
Substance Name:
Apis Mellifera; Arnica Montana Whole; Baptisia Tinctoria Root; Benzoic Acid; Bryonia Alba Root; Colchicum Autumnale Bulb; Echinacea Angustifolia Whole; Eucalyptus Globulus Leaf; Eupatorium Perfoliatum Flowering Top; Mercurialis Perennis Whole; Solanum Dulcamara Top; Solanum Nigrum Whole; Toxicodendron Pubescens Leaf
Usage Information:
For temporary relief of inflamed painful or stiff joints, muscle pain, headache, cough, or fever.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of inflamed painful or stiff joints, muscle pain, headache, cough, or fever.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742130301
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.
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:
07-10-2018
End Marketing Date:
12-01-2028
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 43742-1303-1?

The NDC Packaged Code 43742-1303-1 is assigned to a package of 30 ml in 1 bottle, dropper of Inflammation, 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 43742-1303 included in the NDC Directory?

Yes, Inflammation with product code 43742-1303 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on July 10, 2018.

What is the 11-digit format for NDC 43742-1303-1?

The 11-digit format is 43742130301. 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
5-4-143742-1303-15-4-243742-1303-01