NDC Package 69729-108-20 Histiacil Cough

Dextromethorphan Hydrobromide And Guaifenesin Capsule 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:
69729-108-20
Package Description:
2 BLISTER PACK in 1 BOX / 10 CAPSULE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Histiacil Cough
Non-Proprietary Name:
Dextromethorphan Hydrobromide And Guaifenesin
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
Do not take more than directed - See Overdose warningDo not use for more than 7 days.Do not take more than 6 doses in 24 hoursAdults and children12 years of age & overTake 1 softgel every 4 hours with a full glass of water while symptoms persistChildrenunder 12 years of ageDo not use
11-Digit NDC Billing Format:
69729010820
NDC to RxNorm Crosswalk:
  • RxCUI: 1661740 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG Oral Capsule
  • RxCUI: 1661740 - dextromethorphan hydrobromide 20 MG / guaifenesin 400 MG Oral Capsule
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Opmx Llc
    Dosage Form:
    Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
    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:
    03-01-2022
    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.

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    Frequently Asked Questions

    What is NDC 69729-108-20?

    The NDC Packaged Code 69729-108-20 is assigned to a package of 2 blister pack in 1 box / 10 capsule in 1 blister pack of Histiacil Cough, a human over the counter drug labeled by Opmx Llc. The product's dosage form is capsule and is administered via oral form.

    Is NDC 69729-108 included in the NDC Directory?

    Yes, Histiacil Cough with product code 69729-108 is active and included in the NDC Directory. The product was first marketed by Opmx Llc on March 01, 2022 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 69729-108-20?

    The 11-digit format is 69729010820. 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
    5-3-269729-108-205-4-269729-0108-20