Daytime Cold And Flu Liquid
NDC Package 21130-947-06

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Daytime Cold And Flu (acetaminophen, dextromethorphan hydrobromide, phenylephrine hcl) liquids is uses temporarily relieves common cold/flu symptoms: nasal congestioncough due to minor throat & bronchial irritationsore throatheadacheminor aches & painsfever. This formulation utilizes a liquid delivery system. Marketed by Better Living Brands, Llc, this product is identified by NDC 21130-947 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
21130-947-06
Package Description
236 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
21130094706
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
Daytime Cold And Flu
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hcl
Substance Name
Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
Uses temporarily relieves common cold/flu symptoms: nasal congestioncough due to minor throat & bronchial irritationsore throatheadacheminor aches & painsfever

Regulatory & Marketing

Labeler Name
Better Living Brands, Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-11-2026
Listing Expiration
12-31-2027
Exclude Flag
N
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 21130-947-06 identifies a specific commercial package of 236 ml in 1 bottle of Daytime Cold And Flu, a human over the counter drug labeled by Better Living Brands, Llc. This liquid is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide; phenylephrine hydrochloride 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 Better Living Brands, Llc on April 11, 2026. The current certification is valid through December 31, 2027.

How is this Better Living Brands, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 21130094706. 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)
21130-947-06
11-Digit CMS (5-4-2)
21130-0947-06

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