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  5. NDC Package Code: 69842-952-02 Cvs Itch Relief

NDC Package 69842-952-02 Cvs Itch Relief

Diphenhydramine Hcl,Zinc Acetate Spray 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:
69842-952-02
Package Description:
59 mL in 1 BOTTLE, SPRAY
Product Code:
69842-952
Proprietary Name:
Cvs Itch Relief
Non-Proprietary Name:
Diphenhydramine Hcl, 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:
69842095202
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
59 ML
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
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
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):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
part348
Marketing Category:
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date:
04-14-2014
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 69842-952-02?

The NDC Packaged Code 69842-952-02 is assigned to a package of 59 ml in 1 bottle, spray of Cvs Itch Relief, a human over the counter drug labeled by Cvs. The product's dosage form is spray and is administered via topical form.This product is billed per "ML" milliliter and contains an estimated amount of 59 billable units per package.

Is NDC 69842-952 included in the NDC Directory?

Yes, Cvs Itch Relief with product code 69842-952 is active and included in the NDC Directory. The product was first marketed by Cvs on April 14, 2014 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 69842-952-02?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 59.

What is the 11-digit format for NDC 69842-952-02?

The 11-digit format is 69842095202. 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
5-3-269842-952-025-4-269842-0952-02