Sleepaid Softgels Capsule, Liquid Filled
NDC Package 72090-023-01
Package Information
Sleepaid Softgels (diphenhydramine hydrochloride) capsules is adults and children 12 years of age and over: 1 softgel (50 mg) at bedtime if needed, or as directed by a doctor. This formulation utilizes a capsule, liquid filled delivery system. Marketed by Pioneer Life Sciences, Llc, this product is identified by NDC 72090-023 and is authorized under FDA application M010.
Identification & Billing
- RxCUI: 1020477 - diphenhydrAMINE HCl 50 MG Oral Capsule
- RxCUI: 1020477 - diphenhydramine hydrochloride 50 MG Oral Capsule
- RxCUI: 1020477 - diphenhydramine HCl 50 MG Oral Capsule
Clinical Specifications
- Oral - Administration to or by way of the mouth.
- Oral - Administration to or by way of the mouth.
Regulatory & Marketing
Hierarchy Structure
- 72090 - Pioneer Life Sciences, Llc
- 72090-023 - Sleepaid Softgels
- 72090-023-01 - 180 CAPSULE, LIQUID FILLED in 1 BOTTLE
- 72090-023 - Sleepaid Softgels
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.
Other Available Packages
The following commercial packages are registered under the same Product NDC (72090-023). 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 72090-023-01 identifies a specific commercial package of 180 capsule, liquid filled in 1 bottle of Sleepaid Softgels, a human over the counter drug labeled by Pioneer Life Sciences, Llc. This capsule, liquid filled is formulated for oral use and contains diphenhydramine hydrochloride as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Pioneer Life Sciences, Llc on April 25, 2024. The current certification is valid through December 31, 2026.
How is this Pioneer Life Sciences, Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 72090002301. 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.