Meijer Nighttime Sleep Aid Softgel Capsule, Liquid Filled
NDC Package 79481-0779-8
Package Information
Meijer Nighttime Sleep Aid Softgel (diphenhydramine hydrochloride) capsules is • take only one dose (2 softgels) per day (24 hours) adults and children 12 years and over take 2 softgels at bedtime if needed or as directed by a doctor children under 12 years do not use. This formulation utilizes a capsule, liquid filled delivery system. Marketed by Meijer, Inc., this product is identified by NDC 79481-0779 and is authorized under FDA application M010.
Identification & Billing
- RxCUI: 1049909 - diphenhydrAMINE HCl 25 MG Oral Capsule
- RxCUI: 1049909 - diphenhydramine hydrochloride 25 MG Oral Capsule
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 79481 - Meijer, Inc.
- 79481-0779 - Meijer Nighttime Sleep Aid Softgel
- 79481-0779-8 - 4 BLISTER PACK in 1 CARTON / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
- 79481-0779 - Meijer Nighttime Sleep Aid Softgel
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 (79481-0779). 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 79481-0779-8 identifies a specific commercial package of 4 blister pack in 1 carton / 12 capsule, liquid filled in 1 blister pack of Meijer Nighttime Sleep Aid Softgel, a human over the counter drug labeled by Meijer, Inc.. 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 Meijer, Inc. on June 27, 2024. The current certification is valid through December 31, 2026.
How is this Meijer, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 79481077908. 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.