NDC Package 69536-335-04 Dimetapp Multi-symptom Cold And Flu

Acetaminophen,Diphenhydramine Hydrochloride Solution Oral - View Billable Units, 11-Digit Format, RxNorm

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:
69536-335-04
Package Description:
1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Dimetapp Multi-symptom Cold And Flu
Non-Proprietary Name:
Acetaminophen, Diphenhydramine Hydrochloride
Substance Name:
Acetaminophen; Diphenhydramine Hydrochloride
Usage Information:
Do not exceed recommended dosage. Taking more than the recommended dose (overdose) may cause serious liver damage.measure only with dosage cup providedkeep dosage cup with productmL = milliliteragedoseadults and children 12 years and over20 mL every 4 hours do not take more than 6 doses in any 24-hour period children 6 to under 12 years10 mL every 4 hours do not give more than 5 doses in any 24-hour period children under 6 yearsdo not use
11-Digit NDC Billing Format:
69536033504
NDC to RxNorm Crosswalk:
  • RxCUI: 2683420 - acetaminophen 320 MG / diphenhydrAMINE HCl 12.5 MG in 10 mL Oral Solution
  • RxCUI: 2683420 - acetaminophen 32 MG/ML / diphenhydramine hydrochloride 1.25 MG/ML Oral Solution
  • RxCUI: 2683420 - acetaminophen 320 MG / diphenhydramine HCl 12.5 MG per 10 mL Oral Solution
  • RxCUI: 2683420 - APAP 32 MG/ML / diphenhydramine hydrochloride 1.25 MG/ML Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Foundation Consumer Healthcare
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-01-2024
    Listing Expiration Date:
    12-31-2025
    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 69536-335-04?

    The NDC Packaged Code 69536-335-04 is assigned to a package of 1 bottle in 1 carton / 118 ml in 1 bottle of Dimetapp Multi-symptom Cold And Flu, a human over the counter drug labeled by Foundation Consumer Healthcare. The product's dosage form is solution and is administered via oral form.

    Is NDC 69536-335 included in the NDC Directory?

    Yes, Dimetapp Multi-symptom Cold And Flu with product code 69536-335 is active and included in the NDC Directory. The product was first marketed by Foundation Consumer Healthcare on June 01, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69536-335-04?

    The 11-digit format is 69536033504. 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
    5-3-269536-335-045-4-269536-0335-04