NDC Package 69842-235-27 Itch Relief

Diphenhydramine Hcl And Zinc Acetate Aerosol, Spray Topical - 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:
69842-235-27
Package Description:
76 g in 1 CANISTER
Product Code:
Proprietary Name:
Itch Relief
Non-Proprietary Name:
Diphenhydramine Hcl And Zinc Acetate
Substance Name:
Diphenhydramine Hydrochloride; Zinc Acetate
Usage Information:
Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times dailychildren under 2 years of age: ask a doctor
11-Digit NDC Billing Format:
69842023527
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
76 GM
NDC to RxNorm Crosswalk:
  • RxCUI: 1053138 - diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Spray
  • RxCUI: 1053138 - diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Spray
  • RxCUI: 1053138 - diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Spray
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Cvs Pharmacy
    Dosage Form:
    Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    02-01-2019
    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 69842-235-27?

    The NDC Packaged Code 69842-235-27 is assigned to a package of 76 g in 1 canister of Itch Relief, a human over the counter drug labeled by Cvs Pharmacy. The product's dosage form is aerosol, spray and is administered via topical form.This product is billed per "GM" gram and contains an estimated amount of 76 billable units per package.

    Is NDC 69842-235 included in the NDC Directory?

    Yes, Itch Relief with product code 69842-235 is active and included in the NDC Directory. The product was first marketed by Cvs Pharmacy on February 01, 2019 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 69842-235-27?

    The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 76.

    What is the 11-digit format for NDC 69842-235-27?

    The 11-digit format is 69842023527. 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
    5-3-269842-235-275-4-269842-0235-27