Sunmark Junior Rapid Melts
NDC Package 49348-063-04

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.

Sunmark Junior Rapid Melts is this product does not contain directions or complete warnings for adult dosedo not give more than directed (see overdose warning)find right dose on chart below. Marketed by Mckesson, this product is identified by NDC 49348-063 and is authorized under FDA application part343.

Identification & Billing

NDC Package Code
49348-063-04
Package Description
4 BLISTER PACK in 1 CARTON / 6 TABLET, CHEWABLE in 1 BLISTER PACK
Product Code
49348-063
11-Digit Billing Format
49348006304
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
4 EA
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Sunmark Junior Rapid Melts
Dosage Form
-
Usage Information
This product does not contain directions or complete warnings for adult dosedo not give more than directed (see overdose warning)find right dose on chart below. If possible, use weight to dose; otherwise, use age.dissolve in mouth, or chew before swallowingif needed, repeat dose every 4 hours while symptoms lastdo not give more than 5 times in 24 hoursdo not give more than 5 days unless directed by a doctor. Weight (lb) Age (yr) Tablets under 48 lbs under 6 years ask a doctor 48-59 lbs 6-8 years 2 60-71 lbs 9-10 years 2 1/2 72-95 lbs 11 years 3

Regulatory & Marketing

Labeler Name
Mckesson
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
08-01-2013
Listing Expiration
12-31-2019
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 49348-063-04 identifies a specific commercial package of 4 blister pack in 1 carton / 6 tablet, chewable in 1 blister pack of Sunmark Junior Rapid Melts, labeled by Mckesson. This product is billed for "EA" each discreet unit and contains an estimated amount of 4 billable units per package. 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 Mckesson on August 01, 2013. The current certification is valid through December 31, 2019.

How is this Mckesson product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49348006304. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 4 total billable units per package. 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)
49348-063-04
11-Digit CMS (5-4-2)
49348-0063-04

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