Sanatos Liquid
NDC Package 55758-415-06
Package Information
Sanatos (acetaminophen, dextromethorphan hbr) liquids is use only dosing cup providedshake well before useif you are taking other cold/flu products, read complete labeling before dosingadults & children 12 years & over30 mL every 4 hours, do not exceed (child) 4 doses and (adult) 6 doses per 24 hours children under 12 years of agedo not use. This formulation utilizes a liquid delivery system. Marketed by Pharmadel Llc, this product is identified by NDC 55758-415 and is authorized under FDA application M013.
Identification & Billing
- RxCUI: 2604561 - acetaminophen 650 MG / dextromethorphan HBr 20 MG in 30 mL Oral Solution
- RxCUI: 2604561 - acetaminophen 21.7 MG/ML / dextromethorphan hydrobromide 0.667 MG/ML Oral Solution
- RxCUI: 2604561 - acetaminophen 325 MG / dextromethorphan HBr 10 MG per 15 ML Oral Solution
- RxCUI: 2604561 - acetaminophen 650 MG / dextromethorphan HBr 20 MG per 30 ML Oral Solution
- RxCUI: 2604561 - APAP 21.7 MG/ML / dextromethorphan hydrobromide 0.667 MG/ML Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 55758 - Pharmadel Llc
- 55758-415 - Sanatos
- 55758-415-06 - 177 mL in 1 BOTTLE, PLASTIC
- 55758-415 - Sanatos
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 55758-415-06 identifies a specific commercial package of 177 ml in 1 bottle, plastic of Sanatos Multi Symptom Daytime, a human over the counter drug labeled by Pharmadel Llc. This liquid 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 Pharmadel Llc on December 01, 2023. The current certification is valid through December 31, 2026.
How is this Pharmadel Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 55758041506. 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.