Night Time Cold And Flu Relief Capsule, Liquid Filled
NDC Package 11822-3335-5
Package Information
Night Time Cold And Flu Relief (acetaminophen, dextromethorphan hbr, doxylamine succinate) capsules is do not take more than directed (see Overdose warning)do not take more than 4 doses in 24 hours adults and children 12 years and over: take 2 softgels with water every 6 hours swallow whole; do not crush, chew, or dissolve children under 12 years: do not use when using other Daytime or Nighttime products, carefully read each label to insure correct dosing. This formulation utilizes a capsule, liquid filled delivery system. Marketed by Rite Aid Corporation, this product is identified by NDC 11822-3335 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG Oral Capsule
- RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan hydrobromide 15 MG / doxylamine succinate 6.25 MG Oral Capsule
- RxCUI: 1094549 - APAP 325 MG / dextromethorphan hydrobromide 15 MG / doxylamine succinate 6.25 MG Oral Capsule
Clinical Specifications
- Antihistamine - [EPC] (Established Pharmacologic Class)
- Histamine Receptor Antagonists - [MoA] (Mechanism of Action)
- Sigma-1 Agonist - [EPC] (Established Pharmacologic Class)
- Sigma-1 Receptor Agonists - [MoA] (Mechanism of Action)
- Uncompetitive N-methyl-D-aspartate Receptor Antagonist - [EPC] (Established Pharmacologic Class)
- Uncompetitive NMDA Receptor Antagonists - [MoA] (Mechanism of Action)
Regulatory & Marketing
Hierarchy Structure
- 11822 - Rite Aid Corporation
- 11822-3335 - Night Time Cold And Flu Relief
- 11822-3335-5 - 24 BLISTER PACK in 1 CARTON / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
- 11822-3335 - Night Time Cold And Flu 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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 11822-3335-5 identifies a specific commercial package of 24 blister pack in 1 carton / 1 capsule, liquid filled in 1 blister pack of Night Time Cold And Flu Relief Multi Symptom, a human over the counter drug labeled by Rite Aid Corporation. This capsule, liquid filled is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide; doxylamine succinate 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 Rite Aid Corporation on May 29, 2020.
How is this Rite Aid Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 11822333505. 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.