Boardwalk Hand Sanitizer
NDC Package 71906-700-08
Package Information
Boardwalk Hand Sanitizer is a . Marketed by Essendant Co., this product is identified by NDC 71906-700 and is authorized under FDA application 505G(a)(3).
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 71906 - Essendant Co.
- 71906-700 - Boardwalk Hand Sanitizer
- 71906-700-08 - 236 mL in 1 BOTTLE
- 71906-700 - Boardwalk Hand Sanitizer
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 71906-700-08 identifies a specific commercial package of 236 ml in 1 bottle of Boardwalk Hand Sanitizer, labeled by Essendant Co.. 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 Essendant Co. on August 30, 2015. The current certification is valid through March 31, 2023.
How is this Essendant Co. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 71906070008. 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 Product segment to maintain the 5-4-2 structure.