Cetirizine Hydrochloride (allergy) Tablet
NDC Package 69842-237-91

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Cetirizine Hydrochloride (allergy) (cetirizine hydrochloride) tablets is adults and children 6 years and overone 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours.  A 5 mg product may be appropriate for less severe symptoms.adults 65 years and over ask a doctorchildren under 6 years of age ask a doctorconsumers with liver or kidney diseaseask a doctor. This formulation utilizes a tablet delivery system. Marketed by Cvs Pharmacy, Inc., this product is identified by NDC 69842-237 and is authorized under FDA application ANDA090760.

Identification & Billing

NDC Package Code
69842-237-91
Package Description
1 BOTTLE in 1 CARTON / 30 TABLET in 1 BOTTLE
Product Code
69842-237
11-Digit Billing Format
69842023791
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Cetirizine Hydrochloride (allergy)
Non-Proprietary Name
Cetirizine Hydrochloride
Substance Name
Cetirizine Hydrochloride
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
CETIRIZINE HYDROCHLORIDE 10 mg/1
Pharmacologic Class
Usage Information
Adults and children 6 years and overone 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours.  A 5 mg product may be appropriate for less severe symptoms.adults 65 years and over ask a doctorchildren under 6 years of age ask a doctorconsumers with liver or kidney diseaseask a doctor

Regulatory & Marketing

Labeler Name
Cvs Pharmacy, Inc.
Product Type
Human Otc Drug
FDA Application #
ANDA090760
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
07-26-2019
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (69842-237). Click a package code to view its specific billing and regulatory data.

69842-237-01
1 BLISTER PACK in 1 CARTON / 14 TABLET in 1 BLISTER PACK
69842-237-09
1 BOTTLE in 1 CARTON / 30 TABLET in 1 BOTTLE
69842-237-17
1 BOTTLE in 1 CARTON / 45 TABLET in 1 BOTTLE
69842-237-19
1 BOTTLE in 1 CARTON / 90 TABLET in 1 BOTTLE
69842-237-23
1 BOTTLE in 1 CARTON / 120 TABLET in 1 BOTTLE
69842-237-39
365 TABLET in 1 BOTTLE
69842-237-45
2 BOTTLE in 1 CARTON / 120 TABLET in 1 BOTTLE
69842-237-54
1 BOTTLE in 1 CARTON / 70 TABLET in 1 BOTTLE
69842-237-57
1 BLISTER PACK in 1 CARTON / 5 TABLET in 1 BLISTER PACK
69842-237-60
1 BLISTER PACK in 1 CARTON / 5 TABLET in 1 BLISTER PACK

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 69842-237-91 identifies a specific commercial package of 1 bottle in 1 carton / 30 tablet in 1 bottle of Cetirizine Hydrochloride (allergy), a human over the counter drug labeled by Cvs Pharmacy, Inc.. This tablet is formulated for oral use and contains cetirizine hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Cvs Pharmacy, Inc. on July 26, 2019. The current certification is valid through December 31, 2026.

How is this Cvs Pharmacy, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69842023791. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
69842-237-91
11-Digit CMS (5-4-2)
69842-0237-91

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.