Senna Plus
NDC Package 21695-722-00
Package Information
Senna Plus is ° Take preferably at bedtime or as directed by a doctor ° if you do not have a comfortable bowel movement by the second day, increase dose by one table (do not exceed the maximum dosage) or decrease dose until you are comfortable.Adults & children over 12 years: 2 tablets once a day (maximum dosage, 4 tablets twice a day)Children 6 to under 12 years: 1 tablet once a day (maximum dosage, 2 tablets twice a day)Children 2 to under 6 years: 1.2 tablet once a day (maximum dosage, 1 tablet twice a day)Children under 2 years: do not use. Marketed by Rebel Distributors Corp, this product is identified by NDC 21695-722 and is authorized under FDA application part334.
Identification & Billing
- RxCUI: 312935 - sennosides 8.6 MG Oral Tablet
- RxCUI: 312935 - sennosides, USP 8.6 MG Oral Tablet
- RxCUI: 312935 - sennosides A and B 8.6 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 21695 - Rebel Distributors Corp
- 21695-722 - Senna Plus
- 21695-722-00 - 100 TABLET in 1 BOTTLE
- 21695-722 - Senna Plus
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.
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Other Available Packages
The following commercial packages are registered under the same Product NDC (21695-722). Click a package code to view its specific billing and regulatory data.
* 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 21695-722-00 identifies a specific commercial package of 100 tablet in 1 bottle of Senna Plus, labeled by Rebel Distributors Corp. This product is billed for "EA" each discreet unit and contains an estimated amount of 100 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 Rebel Distributors Corp on July 10, 2009. The current certification is valid through December 31, 2017.
How is this Rebel Distributors Corp product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 21695072200. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 100 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.