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  5. NDC Package Code: 69729-785-06 Rompe Tos X Adults

NDC Package 69729-785-06 Rompe Tos X Adults

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
69729-785-06
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 177 mL in 1 BOTTLE, PLASTIC
Product Code:
69729-785
Proprietary Name:
Rompe Tos X Adults
Usage Information:
Do not take more than directed (see Overdose warning)do not take more than 6 doses in any 24 hour periodmeasure only with dosing cup provideddo not use dosing cup with other productsdose as follows or as directed by a doctormL = millilitertsp = teaspoonfulAgeDoseadults and children 12 years of age and older20 mL in dosing cup provided every 4 hoursChildren under 12 years of agedo not use
11-Digit NDC Billing Format:
69729078506
NDC to RxNorm Crosswalk:
  • RxCUI: 1790651 - acetaminophen 250 MG / dextromethorphan HBr 13.33 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG in 10 mL Oral Solution
  • RxCUI: 1790651 - acetaminophen 25 MG/ML / dextromethorphan hydrobromide 1.33 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
  • RxCUI: 1790651 - acetaminophen 250 MG / dextromethorphan HBr 13.33 MG / guaifenesin 200 MG / phenylephrine HCl 5 MG per 10 ML Oral Solution
  • RxCUI: 1790651 - acetaminophen 500 MG / dextromethorphan HBr 26.66 MG / guaifenesin 400 MG / phenylephrine HCl 10 MG per 20 ML Oral Solution
  • RxCUI: 1790651 - APAP 25 MG/ML / Dextromethorphan Hydrobromide 1.33 MG/ML / Guaifenesin 20 MG/ML / Phenylephrine Hydrochloride 0.5 MG/ML Oral Solution
Labeler Name:
Opmx Llc
Sample Package:
No
FDA Application Number:
part341
Marketing Category:
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date:
09-18-2023
Listing Expiration Date:
12-31-2024
Exclude Flag:
I
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 69729-785-06?

The NDC Packaged Code 69729-785-06 is assigned to a package of 1 bottle, plastic in 1 carton / 177 ml in 1 bottle, plastic of Rompe Tos X Adults, labeled by Opmx Llc. The product's dosage form is and is administered via form.

Is NDC 69729-785 included in the NDC Directory?

No, Rompe Tos X Adults with product code 69729-785 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Opmx Llc on September 18, 2023 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 69729-785-06?

The 11-digit format is 69729078506. 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
5-3-269729-785-065-4-269729-0785-06