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  5. NDC Package Code: 69968-0459-1 Benadryl Extra Strength Itch Relief

NDC Package 69968-0459-1 Benadryl Extra Strength Itch Relief

Diphenhydramine Hydrochloride And Zinc Acetate Solution Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
69968-0459-1
Package Description:
1 APPLICATOR in 1 CARTON / 14 mL in 1 APPLICATOR
Product Code:
69968-0459
Proprietary Name:
Benadryl Extra Strength Itch Relief
Non-Proprietary Name:
Diphenhydramine Hydrochloride And Zinc Acetate
Substance Name:
Diphenhydramine Hydrochloride; Zinc Acetate
Usage Information:
Do not use more than directedhold stick straight down over affected skin areapress tip of stick repeatedly on affected skin area until liquid flows, then dab sparingly 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:
69968045901
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1294589 - diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Solution
  • RxCUI: 1294589 - diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Solution
  • RxCUI: 1294589 - diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Solution
  • RxCUI: 1294591 - Benadryl 2 % / 0.1 % Topical Solution
  • RxCUI: 1294591 - diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Solution [Benadryl Itch Stopping]
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Johnson & Johnson Consumer Inc.
    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):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • DIPHENHYDRAMINE HYDROCHLORIDE 20 mg/mL
  • ZINC ACETATE 1 mg/mL
    • Pharmacologic Class(es):
  • Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
  • Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
  • Histamine H1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-01-2019
    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 69968-0459-1?

    The NDC Packaged Code 69968-0459-1 is assigned to a package of 1 applicator in 1 carton / 14 ml in 1 applicator of Benadryl Extra Strength Itch Relief, a human over the counter drug labeled by Johnson & Johnson Consumer Inc.. The product's dosage form is solution and is administered via topical form.

    Is NDC 69968-0459 included in the NDC Directory?

    Yes, Benadryl Extra Strength Itch Relief with product code 69968-0459 is active and included in the NDC Directory. The product was first marketed by Johnson & Johnson Consumer Inc. on June 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 69968-0459-1?

    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 69968-0459-1?

    The 11-digit format is 69968045901. 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 5-4-1 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
    5-4-169968-0459-15-4-269968-0459-01