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  5. NDC Package Code: 20276-210-08 Lucky Blue Ice

NDC Package 20276-210-08 Lucky Blue Ice

Menthol Camphor Gel 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:
20276-210-08
Package Description:
227 g in 1 JAR
Product Code:
20276-210
Proprietary Name:
Lucky Blue Ice
Non-Proprietary Name:
Menthol Camphor
Substance Name:
Camphor (synthetic); Menthol
Usage Information:
Apply liberally to painful zones and massage until absorbed into the skin. Repeat daily 3 or 4 times. Keep out of reach of children. Do not apply to children below two years of age.
11-Digit NDC Billing Format:
20276021008
NDC to RxNorm Crosswalk:
  • RxCUI: 1043046 - camphor 0.5 % / menthol 1 % Topical Gel
  • RxCUI: 1043046 - camphor 0.005 MG/MG / menthol 0.01 MG/MG Topical Gel
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Delta Brands Inc
    Dosage Form:
    Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
    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) .5 g/100g
  • MENTHOL 1 g/100g
    • Sample Package:
    No
    FDA Application Number:
    part348
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    11-15-2009
    Listing Expiration Date:
    12-31-2024
    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 20276-210-08?

    The NDC Packaged Code 20276-210-08 is assigned to a package of 227 g in 1 jar of Lucky Blue Ice, a human over the counter drug labeled by Delta Brands Inc. The product's dosage form is gel and is administered via topical form.

    Is NDC 20276-210 included in the NDC Directory?

    Yes, Lucky Blue Ice with product code 20276-210 is active and included in the NDC Directory. The product was first marketed by Delta Brands Inc on November 15, 2009 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 20276-210-08?

    The 11-digit format is 20276021008. 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
    5-3-220276-210-085-4-220276-0210-08