Unishield Pain Zapper
NDC Package 49314-8113-3

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.

Unishield Pain Zapper is usest emporarily relieved minor aches and pains associated with■ headaches ■ muscular aches ■ minor arthritis pain ■ back pain ■ colds ■ toothache ■ menstrual crampsTemporarily reduces fever. Marketed by Unishield, this product is identified by NDC 49314-8113 and is authorized under FDA application part343.

Identification & Billing

NDC Package Code
49314-8113-3
Package Description
50 PACKET in 1 BOX / 2 TABLET in 1 PACKET
Product Code
49314-8113
11-Digit Billing Format
49314811303
RxNorm Crosswalk
  • RxCUI: 359221 - acetaminophen 110 MG / aspirin 162 MG / salicylamide 152 MG / caffeine 32.4 MG Oral Tablet
  • RxCUI: 359221 - acetaminophen 110 MG / aspirin 162 MG / caffeine 32.4 MG / salicylamide 152 MG Oral Tablet
  • RxCUI: 359221 - APAP 110 MG / ASA 162 MG / Caffeine 32.4 MG / salicylamide 152 MG Oral Tablet

Clinical Specifications

Proprietary Name
Unishield Pain Zapper
Dosage Form
-
Usage Information
Usest emporarily relieved minor aches and pains associated with■ headaches ■ muscular aches ■ minor arthritis pain ■ back pain ■ colds ■ toothache ■ menstrual crampsTemporarily reduces fever.

Regulatory & Marketing

Labeler Name
Unishield
FDA Application #
part343
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
03-01-2021
Listing Expiration
12-31-2023
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 49314-8113-3 identifies a specific commercial package of 50 packet in 1 box / 2 tablet in 1 packet of Unishield Pain Zapper, labeled by Unishield. 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 Unishield on March 01, 2021. The current certification is valid through December 31, 2023.

How is this Unishield product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49314811303. 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)
49314-8113-3
11-Digit CMS (5-4-2)
49314-8113-03

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