Lucky
NDC Package 47046-169-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Lucky is ■ adults and children 2 years of age and over: apply a small amount of the product to the cavity and around the gum surrounding the teeth Use up to 4 times daily or as directed by a physician or healthcare provider ■ children under 12 years: should be supervised in the use of this product ■ children under 2 years of age: ask a physician or health care provider. Marketed by Anicare Pharmaceuticals Pvt. Ltd., this product is identified by NDC 47046-169 and is authorized under FDA application part356.

Identification & Billing

NDC Package Code
47046-169-01
Package Description
14 g in 1 TUBE
Product Code
47046-169
11-Digit Billing Format
47046016901
RxNorm Crosswalk
  • RxCUI: 1595155 - benzocaine 20 % / benzalkonium chloride 0.1 % Oral Gel
  • RxCUI: 1595155 - benzalkonium chloride 0.001 MG/MG / benzocaine 0.2 MG/MG Oral Gel
  • RxCUI: 1595155 - benzalkonium chloride 0.1 % / benzocaine 20 % Oral Gel

Clinical Specifications

Proprietary Name
Lucky Oral Pain Relief
Dosage Form
-
Usage Information
■ adults and children 2 years of age and over: apply a small amount of the product to the cavity and around the gum surrounding the teeth Use up to 4 times daily or as directed by a physician or healthcare provider ■ children under 12 years: should be supervised in the use of this product ■ children under 2 years of age: ask a physician or health care provider

Regulatory & Marketing

Labeler Name
Anicare Pharmaceuticals Pvt. Ltd.
FDA Application #
part356
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
06-15-2014
Listing Expiration
12-31-2021
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 47046-169-01 identifies a specific commercial package of 14 g in 1 tube of Lucky Oral Pain Relief, labeled by Anicare Pharmaceuticals Pvt. Ltd.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Anicare Pharmaceuticals Pvt. Ltd. on June 15, 2014. The current certification is valid through December 31, 2021.

How is this Anicare Pharmaceuticals Pvt. Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 47046016901. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
47046-169-01
11-Digit CMS (5-4-2)
47046-0169-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.