Cold And Flu
NDC Package 37835-526-02

11-digit billing NDC: 37835052602
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Cold And Flu is do not take more than directedmL = milliliter; FL OZ = fluid ounceuse only enclosed dosing cup designed for use with this product. Marketed by Bi-mart, this product is identified by NDC 37835-526 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
37835-526-02
Package Description
355 mL in 1 BOTTLE, PLASTIC
Product Code
37835-526
11-Digit Billing Format
37835052602
RxNorm Crosswalk
  • RxCUI: 1113705 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG in 15 mL Oral Solution
  • RxCUI: 1113705 - acetaminophen 21.7 MG/ML / dextromethorphan hydrobromide 0.667 MG/ML / phenylephrine hydrochloride 0.333 MG/ML Oral Solution
  • RxCUI: 1113705 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG per 15 ML Oral Solution
  • RxCUI: 1113705 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG per 30 ML Oral Solution
  • RxCUI: 1113705 - APAP 21.7 MG/ML / dextromethorphan hydrobromide 0.667 MG/ML / phenylephrine hydrochloride 0.333 MG/ML Oral Solution

Clinical Specifications

Proprietary Name
Cold And Flu Daytime
Dosage Form
-
Usage Information
Do not take more than directedmL = milliliter; FL OZ = fluid ounceuse only enclosed dosing cup designed for use with this product. Do not use any other dosing device.do not take more than 5 doses per 24 hoursadults and children 12 years and over30 mL every 4 hourschildren 6 to under 12 years15 mL every 4 hourschildren under 6 yearsdo not use

Regulatory & Marketing

Labeler Name
Bi-mart
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-18-2018
End Marketing Date
04-30-2026
Listing Expiration
04-30-2026
Exclude Flag
D
Sample Package
No

Hierarchy Structure

Code Lineage

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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (37835-526). Click a package code to view its specific billing and regulatory data.

37835-526-30
354 mL in 1 BOTTLE, PLASTIC

* 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 37835-526-02 identifies a specific commercial package of 355 ml in 1 bottle, plastic of Cold And Flu Daytime, labeled by Bi-mart. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Bi-mart on June 18, 2018. The current certification is valid through April 30, 2026.

How is this Bi-mart product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 37835052602. 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:

10-Digit Format (5-3-2)
37835-526-02
11-Digit CMS (5-4-2)
37835-0526-02

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.