Dct
NDC Package 10157-1127-1
Package Information
Dct is a . Marketed by Blistex Inc., this product is identified by NDC 10157-1127 and is authorized under FDA application part352.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 10157 - Blistex Inc.
- 10157-1127 - Dct
- 10157-1127-1 - 1 JAR in 1 BLISTER PACK / 7 g in 1 JAR
- 10157-1127 - Dct
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 10157-1127-1 identifies a specific commercial package of 1 jar in 1 blister pack / 7 g in 1 jar of Dct, labeled by Blistex Inc.. 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 Blistex Inc. on May 08, 2018. The current certification is valid through July 27, 2020.
How is this Blistex Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 10157112701. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.