NDC Package 69842-621-01 Cvs Regular Strength Itch Stopping

Diphenhydramine Hydrochloride,Zinc Acetate Cream 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:
69842-621-01
Package Description:
1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Code:
Proprietary Name:
Cvs Regular Strength Itch Stopping
Non-Proprietary Name:
Diphenhydramine Hydrochloride, Zinc Acetate
Substance Name:
Diphenhydramine Hydrochloride; Zinc Acetate
Usage Information:
Do not use more often than directedadults and children 2 years and older: apply to affected area not more than 3 to 4 times dailychildren under 2 years: ask a doctor
11-Digit NDC Billing Format:
69842062101
NDC to RxNorm Crosswalk:
  • RxCUI: 1292313 - diphenhydrAMINE HCl 1 % / zinc acetate 0.1 % Topical Cream
  • RxCUI: 1292313 - diphenhydramine hydrochloride 10 MG/ML / zinc acetate 1 MG/ML Topical Cream
  • RxCUI: 1292313 - diphenhydramine hydrochloride 1 % / zinc acetate 0.1 % Topical Cream
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Cvs
    Dosage Form:
    Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    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:
    03-17-2014
    Listing Expiration Date:
    12-31-2024
    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 69842-621-01?

    The NDC Packaged Code 69842-621-01 is assigned to a package of 1 tube in 1 carton / 28 g in 1 tube of Cvs Regular Strength Itch Stopping, a human over the counter drug labeled by Cvs. The product's dosage form is cream and is administered via topical form.

    Is NDC 69842-621 included in the NDC Directory?

    Yes, Cvs Regular Strength Itch Stopping with product code 69842-621 is active and included in the NDC Directory. The product was first marketed by Cvs on March 17, 2014 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 69842-621-01?

    The 11-digit format is 69842062101. 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
    5-3-269842-621-015-4-269842-0621-01