Sleep Aid Plus Pain Relief Solution
NDC Package 0363-9074-02
Package Information
Sleep Aid Plus Pain Relief (acetaminophen, diphenhydramine hcl) solution is do not take more than directedmL = milliliter; FL OZ = fluid ounceonly use the dose cup providedadults and children 12 years and over: take 30 mL in the dosing cup provided at bedtime. This formulation utilizes a solution delivery system. Marketed by Walgreen Company, this product is identified by NDC 0363-9074 and is authorized under FDA application M013.
Identification & Billing
- RxCUI: 1092373 - acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG in 15 mL Oral Solution
- RxCUI: 1092373 - acetaminophen 33.3 MG/ML / diphenhydramine hydrochloride 1.67 MG/ML Oral Solution
- RxCUI: 1092373 - acetaminophen 1000 MG / diphenhydramine HCl 50 MG per 30 ML Oral Solution
- RxCUI: 1092373 - acetaminophen 500 MG / diphenhydramine HCl 25 MG per 15 ML Oral Solution
- RxCUI: 1092373 - APAP 33.3 MG/ML / Diphenhydramine Hydrochloride 1.67 MG/ML Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0363 - Walgreen Company
- 0363-9074 - Sleep Aid Plus Pain Relief
- 0363-9074-02 - 355 mL in 1 BOTTLE, PLASTIC
- 0363-9074 - Sleep Aid Plus Pain Relief
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 0363-9074-02 identifies a specific commercial package of 355 ml in 1 bottle, plastic of Sleep Aid Plus Pain Relief, a human over the counter drug labeled by Walgreen Company. This solution is formulated for oral use and contains acetaminophen; 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 Walgreen Company on August 27, 2022. The current certification is valid through December 31, 2027.
How is this Walgreen Company product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00363907402. 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 Labeler segment to maintain the 5-4-2 structure.