NDC Package 0067-2086-01 4 Way Fast Acting

Phenylephrine Hydrochloride Spray Nasal - 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:
0067-2086-01
Package Description:
1 BOTTLE, SPRAY in 1 CARTON / 29.6 mL in 1 BOTTLE, SPRAY
Product Code:
Proprietary Name:
4 Way Fast Acting
Non-Proprietary Name:
Phenylephrine Hydrochloride
Substance Name:
Phenylephrine Hydrochloride
Usage Information:
•adults and children 12 years of age and over: 2 or 3 sprays in each nostril not more often than every 4 hours•children under 12 years of age: ask a doctor•Use instructions: with head in a normal, upright position, put atomizer tip into nostril. Squeeze bottle with firm, quick pressure while inhaling. Wipe nozzle clean after each use.
11-Digit NDC Billing Format:
00067208601
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1087043 - phenylephrine HCl 1 % Nasal Spray
  • RxCUI: 1087043 - phenylephrine hydrochloride 10 MG/ML Nasal Spray
  • RxCUI: 1087043 - phenylephrine hydrochloride 1 % Nasal Spray
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Haleon Us Holdings Llc
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    Administration Route(s):
  • Nasal - Administration to the nose; administered by way of the nose.
  • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-01-2010
    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 0067-2086-01?

    The NDC Packaged Code 0067-2086-01 is assigned to a package of 1 bottle, spray in 1 carton / 29.6 ml in 1 bottle, spray of 4 Way Fast Acting, a human over the counter drug labeled by Haleon Us Holdings Llc. The product's dosage form is spray and is administered via nasal form.

    Is NDC 0067-2086 included in the NDC Directory?

    Yes, 4 Way Fast Acting with product code 0067-2086 is active and included in the NDC Directory. The product was first marketed by Haleon Us Holdings Llc on January 01, 2010 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 NDC billing unit for package 0067-2086-01?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 0067-2086-01?

    The 11-digit format is 00067208601. 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 4-4-2 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
    4-4-20067-2086-015-4-200067-2086-01