Good Neighbor Pharmacy Powder, For Solution
NDC Package 46122-841-59
Package Information
Good Neighbor Pharmacy (acetaminophen, dextromethorphan hbr) powders is •do not use more than directed•take every 6 hours, while symptoms persist•do not take more than 3 packets in 24 hours unless directed by a doctor Age Dose adults and children 12 years of age and over One packet children under 12 years of age do not use▪dissolve contents of one packet into 8 oz. This formulation utilizes a powder, for solution delivery system. Marketed by Amerisource Bergen, this product is identified by NDC 46122-841 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 2636656 - acetaminophen 1000 MG / dextromethorphan hydrobromide 30 MG Powder for Oral Solution
- RxCUI: 2636656 - acetaminophen 1000 MG / dextromethorphan hydrobromide 30 MG Granules for Oral Solution
- RxCUI: 2636656 - APAP 1000 MG / dextromethorphan hydrobromide 30 MG Powder for Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 46122 - Amerisource Bergen
- 46122-841 - Good Neighbor Pharmacy
- 46122-841-59 - 6 PACKET in 1 CARTON / 1 POWDER, FOR SOLUTION in 1 PACKET
- 46122-841 - Good Neighbor Pharmacy
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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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 46122-841-59 identifies a specific commercial package of 6 packet in 1 carton / 1 powder, for solution in 1 packet of Good Neighbor Pharmacy Daytime Flu Relief Max Strength, a human over the counter drug labeled by Amerisource Bergen. This powder, for solution is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide 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 Amerisource Bergen on May 04, 2026. The current certification is valid through December 31, 2027.
How is this Amerisource Bergen product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 46122084159. 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.