Akin Cough Formula Dm Strawberry Banana Liquid
NDC Package 69822-211-04
Package Information
Akin Cough Formula Dm Strawberry Banana (dextromethorphan hydrobromide, guaifenesin) liquids is do not take more than 6 doses in any 24 hours period Adults and children 12 years and over 10 ml (2 teaspoonfuls every 4 hours or as directed by doctor) Children under 12 years do not use. This formulation utilizes a liquid delivery system. Marketed by Southern Sales & Service, Inc., this product is identified by NDC 69822-211 and is authorized under FDA application M012.
Identification & Billing
Clinical Specifications
- Decreased Respiratory Secretion Viscosity - [PE] (Physiologic Effect)
- Expectorant - [EPC] (Established Pharmacologic Class)
- Increased Respiratory Secretions - [PE] (Physiologic Effect)
- 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
- 69822 - Southern Sales & Service, Inc.
- 69822-211 - Akin Cough Formula Dm Strawberry Banana
- 69822-211-04 - 118 mL in 1 BOTTLE
- 69822-211 - Akin Cough Formula Dm Strawberry Banana
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 69822-211-04 identifies a specific commercial package of 118 ml in 1 bottle of Akin Cough Formula Dm Strawberry Banana, a human over the counter drug labeled by Southern Sales & Service, Inc.. This liquid is formulated for topical use and contains dextromethorphan hydrobromide; guaifenesin 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 Southern Sales & Service, Inc. on February 01, 2023. The current certification is valid through December 31, 2026.
How is this Southern Sales & Service, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 69822021104. 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.