Arthritis Pain Reliever
NDC Package 69256-012-35

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Arthritis Pain Reliever is use up to 21 days unless directed by your doctor. Marketed by Harris Teeter, Llc, this product is identified by NDC 69256-012 and is authorized under FDA application ANDA208077.

Identification & Billing

NDC Package Code
69256-012-35
Package Description
1 TUBE in 1 CARTON / 100 g in 1 TUBE
Product Code
11-Digit Billing Format
69256001235

Clinical Specifications

Proprietary Name
Arthritis Pain Reliever
Dosage Form
-
Usage Information
Use up to 21 days unless directed by your doctor. Not for strains, sprains, bruises or sports injuries.This product has not been shown to work for these types of injuries. Daily Per Dose For your arthritis pain:Use 4 times per day every dayDo not use on more than 2 body areas at the same time Use ENCLOSED DOSING CARD to measure a dose For each upper body area (hand, wrist, or elbow) – Squeeze out 2.25 inches (2 grams)For each lower body area (foot, ankle, or knee) – Squeeze out 4.5 inches (4 grams) Read the enclosed User Guide for complete instructions:use only as directeddo not use more than directed or for longer than directedapply only to clean, dry skin that does not have any cuts, open wounds, infections, or rashesdo not apply in same areas as any other productdo not apply with external heat such as a heating paddo not apply a bandage over the treated areastore ENCLOSED DOSING CARD with your Diclofenac Sodium Topical Gel, 1%. The dosing card is re-usable.

Regulatory & Marketing

Labeler Name
Harris Teeter, Llc
FDA Application #
ANDA208077
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
01-29-2021
End Marketing Date
05-29-2026
Listing Expiration
05-29-2026
Exclude Flag
D
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (69256-012). Click a package code to view its specific billing and regulatory data.

1 TUBE in 1 CARTON / 50 g in 1 TUBE

* 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 69256-012-35 identifies a specific commercial package of 1 tube in 1 carton / 100 g in 1 tube of Arthritis Pain Reliever, labeled by Harris Teeter, Llc. 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 Harris Teeter, Llc on January 29, 2021. The current certification is valid through May 29, 2026.

How is this Harris Teeter, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69256001235. 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)
69256-012-35
11-Digit CMS (5-4-2)
69256-0012-35

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