1. Home
  2. Labeler Index
  3. Bi-mart
  4. 37835-527
  5. NDC Package Code: 37835-527-12 Daytime Cold And Flu

NDC Package 37835-527-12 Daytime Cold And Flu

Acetaminophen,Dextromethorphan Hbr,Phenylephrine Hcl Liquid Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
37835-527-12
Package Description:
355 mL in 1 BOTTLE
Product Code:
37835-527
Proprietary Name:
Daytime Cold And Flu
Non-Proprietary Name:
Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride
Usage Information:
Take only as directed (see Overdose warning)measure only with dose cup provided and keep dose cup with product mL=mililiterdo not exceed 4 doses per 24 hoursAgeDoseadults & children 12 years and over30 mL every 4 hours children 6 to under 12 years15 mL every 4 hours children under 6 yearsdo not use 
11-Digit NDC Billing Format:
37835052712
NDC to 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
Product Type:
Human Otc Drug
Labeler Name:
Bi-mart
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(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
05-01-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 37835-527-12?

The NDC Packaged Code 37835-527-12 is assigned to a package of 355 ml in 1 bottle of Daytime Cold And Flu, a human over the counter drug labeled by Bi-mart. The product's dosage form is liquid and is administered via oral form.

Is NDC 37835-527 included in the NDC Directory?

Yes, Daytime Cold And Flu with product code 37835-527 is active and included in the NDC Directory. The product was first marketed by Bi-mart on May 01, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 37835-527-12?

The 11-digit format is 37835052712. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-237835-527-125-4-237835-0527-12