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  5. NDC Package Code: 79804-282-03 Pain Relief Roll On

NDC Package 79804-282-03 Pain Relief Roll On

Topical Analgesic Liquid Topical - 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:
79804-282-03
Package Description:
87 g in 1 PACKAGE
Product Code:
79804-282
Proprietary Name:
Pain Relief Roll On
Non-Proprietary Name:
Topical Analgesic
Substance Name:
Camphor (synthetic); Capsaicin; Menthol
Usage Information:
Adults and Children over 12 years old: Apply to afected area - do not apply more than 4 times daily. Children 12 years or younger: consult a doctor
11-Digit NDC Billing Format:
79804028203
NDC to RxNorm Crosswalk:
  • RxCUI: 2610122 - camphor 5 % / capsaicin 0.025 % / menthol 6 % Topical Solution
  • RxCUI: 2610122 - camphor 50 MG/ML / capsaicin 0.25 MG/ML / menthol 60 MG/ML Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Eagle Labs 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):
  • 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):
  • CAMPHOR (SYNTHETIC) .05 g/g
  • CAPSAICIN .00025 g/g
  • MENTHOL .06 g/g
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    11-07-2022
    Listing Expiration Date:
    12-31-2025
    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 79804-282-03?

    The NDC Packaged Code 79804-282-03 is assigned to a package of 87 g in 1 package of Pain Relief Roll On, a human over the counter drug labeled by Eagle Labs Inc. The product's dosage form is liquid and is administered via topical form.

    Is NDC 79804-282 included in the NDC Directory?

    Yes, Pain Relief Roll On with product code 79804-282 is active and included in the NDC Directory. The product was first marketed by Eagle Labs Inc on November 07, 2022 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 79804-282-03?

    The 11-digit format is 79804028203. 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 5-3-2 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
    5-3-279804-282-035-4-279804-0282-03