1. Home
  2. Labeler Index
  3. The Magni Company
  4. 43689-0044
  5. NDC Package Code: 43689-0044-1 Pain And Inflammation Relief Foam

NDC Package 43689-0044-1 Pain And Inflammation Relief Foam

Calendula Officinalis,Croton Tiglium,Natrum Muriaticum,Plantago Major,Rhus - 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:
43689-0044-1
Package Description:
118 mL in 1 BOTTLE, PUMP
Product Code:
43689-0044
Proprietary Name:
Pain And Inflammation Relief Foam
Non-Proprietary Name:
Calendula Officinalis, Croton Tiglium, Natrum Muriaticum, Plantago Major, Rhus Tox, Sarsaparilla (smilax Regelii)
Substance Name:
Calendula Officinalis Flowering Top; Croton Tiglium Seed; Plantago Major Whole; Smilax Ornata Root; Sodium Chloride; Toxicodendron Pubescens Leaf
Usage Information:
Temporary relief from minor aches and pains of sore muscles and joints due to inflammation associated with: • Arthritis• Strains• Sprains• Trauma Temporary relief from minor aches and pains of sore muscles and joints due to inflammation associated with:• Arthritis• Strains• Sprains• Trauma
11-Digit NDC Billing Format:
43689004401
Product Type:
Human Otc Drug
Labeler Name:
The Magni Company
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):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • CALENDULA OFFICINALIS FLOWERING TOP 12 [hp_X]/mL
  • CROTON TIGLIUM SEED 30 [hp_X]/mL
  • PLANTAGO MAJOR WHOLE 30 [hp_X]/mL
  • SMILAX ORNATA ROOT 30 [hp_X]/mL
  • SODIUM CHLORIDE 30 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 30 [hp_X]/mL
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    08-03-2020
    End Marketing Date:
    11-18-2025
    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 43689-0044-1?

    The NDC Packaged Code 43689-0044-1 is assigned to a package of 118 ml in 1 bottle, pump of Pain And Inflammation Relief Foam, a human over the counter drug labeled by The Magni Company. The product's dosage form is liquid and is administered via topical form.

    Is NDC 43689-0044 included in the NDC Directory?

    Yes, Pain And Inflammation Relief Foam with product code 43689-0044 is active and included in the NDC Directory. The product was first marketed by The Magni Company on August 03, 2020.

    What is the 11-digit format for NDC 43689-0044-1?

    The 11-digit format is 43689004401. 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
    5-4-143689-0044-15-4-243689-0044-01