1. Home
  2. Labeler Index
  3. Liddell Laboratories, Inc.
  4. 50845-0280
  5. NDC Package Code: 50845-0280-1 Derma Pain

NDC Package 50845-0280-1 Derma Pain

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:
50845-0280-1
Package Description:
30 mL in 1 BOTTLE, SPRAY
Product Code:
50845-0280
Proprietary Name:
Derma Pain
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:
May temporarily relieve shooting pain, itching, burning, and sensitivity to touch, with or after eruptions and blisters.****Clains based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve shooting pain, itching, burning, and sensitivity to touch, with or after eruptions and blisters.****Clains based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
11-Digit NDC Billing Format:
50845028001
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):
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):
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
06-29-2022
End Marketing Date:
03-09-2027
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 50845-0280-1?

The NDC Packaged Code 50845-0280-1 is assigned to a package of 30 ml in 1 bottle, spray of Derma Pain, a human over the counter drug labeled by Liddell Laboratories, Inc.. The product's dosage form is spray and is administered via topical form.

Is NDC 50845-0280 included in the NDC Directory?

Yes, Derma Pain with product code 50845-0280 is active and included in the NDC Directory. The product was first marketed by Liddell Laboratories, Inc. on June 29, 2022.

What is the 11-digit format for NDC 50845-0280-1?

The 11-digit format is 50845028001. 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
5-4-150845-0280-15-4-250845-0280-01