All Day Pain Relief
NDC Package 68210-0030-1

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.

All Day Pain Relief is do not take more than directedthe smallest effective dose should be useddrink a full glass of water with each doseAdults and Children 12 years and older:take 1 tablet every 8 to 12 hours while symptoms lastfor the first dose you may take 2 tablets within the first hourdo not exceed 2 tablets in any 8 to 12 hour perioddo not exceed 3 tablets in a 24-hour periodChildren under 12 years:ask a doctor. Marketed by Spirit Pharmaceuticals Llc, this product is identified by NDC 68210-0030 and is authorized under FDA application ANDA090545.

Identification & Billing

NDC Package Code
68210-0030-1
Package Description
1 BOTTLE in 1 CARTON / 15 TABLET in 1 BOTTLE
Product Code
68210-0030
11-Digit Billing Format
68210003001
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
All Day Pain Relief
Dosage Form
-
Usage Information
Do not take more than directedthe smallest effective dose should be useddrink a full glass of water with each doseAdults and Children 12 years and older:take 1 tablet every 8 to 12 hours while symptoms lastfor the first dose you may take 2 tablets within the first hourdo not exceed 2 tablets in any 8 to 12 hour perioddo not exceed 3 tablets in a 24-hour periodChildren under 12 years:ask a doctor

Regulatory & Marketing

Labeler Name
Spirit Pharmaceuticals Llc
FDA Application #
ANDA090545
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
04-11-2018
Listing Expiration
12-31-2022
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 68210-0030-1 identifies a specific commercial package of 1 bottle in 1 carton / 15 tablet in 1 bottle of All Day Pain Relief, labeled by Spirit Pharmaceuticals 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 Spirit Pharmaceuticals Llc on April 11, 2018. The current certification is valid through December 31, 2022.

How is this Spirit Pharmaceuticals Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68210003001. 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 (5-4-1)
68210-0030-1
11-Digit CMS (5-4-2)
68210-0030-01

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