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  4. NDC Product Code: 0363-2088 Wal-zyr Cetirizine Hydrochloride

NDC 0363-2088 Wal-zyr Cetirizine Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0363-2088?
  5. Wal-zyr Cetirizine Hydrochloride Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
0363-2088
Proprietary Name:
Wal-zyr Cetirizine Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walgreen Company
Labeler Code:
0363
Product Label ID:
e28ed917-e699-4255-8710-0747fc25dd6f
Start Marketing Date: [9]
04-22-2008
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - COLORLESS TO SLIGHTLY YELLOW)
Flavor(s):
GRAPE (C73391)

Product Packages

NDC Code 0363-2088-02

Package Description: 1 BOTTLE in 1 CARTON / 240 mL in 1 BOTTLE

NDC Code 0363-2088-05

Package Description: 10 POUCH in 1 CARTON / 1 VIAL, SINGLE-DOSE in 1 POUCH / 5 mL in 1 VIAL, SINGLE-DOSE

NDC Code 0363-2088-08

Package Description: 1 BOTTLE in 1 CARTON / 120 mL in 1 BOTTLE

Product Details

What is NDC 0363-2088?

The NDC code 0363-2088 is assigned by the FDA to the product Wal-zyr Cetirizine Hydrochloride which is product labeled by Walgreen Company. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 0363-2088-02 1 bottle in 1 carton / 240 ml in 1 bottle, 0363-2088-05 10 pouch in 1 carton / 1 vial, single-dose in 1 pouch / 5 ml in 1 vial, single-dose, 0363-2088-08 1 bottle in 1 carton / 120 ml in 1 bottle. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Wal-zyr Cetirizine Hydrochloride?

Medicine should be dispensed directly into mouth using the enclosed pre-filled vial(s).adults and children 6 years and over1 pre-filled (5 mL) or 2 pre-filled vials (10 mL) once daily depending upon severity of symptoms; do not take more than 2 pre-filled vials (10 mL) in 24 hours.adults 65 years and over1 pre-filled vial (5 mL) once daily; do not take more than 1 pre-filled vial (5 mL) in 24 hours.children under 6 years of ageask a doctorConsumer with liver or kidney diseaseask a doctor

Which are Wal-zyr Cetirizine Hydrochloride UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Wal-zyr Cetirizine Hydrochloride Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Wal-zyr Cetirizine Hydrochloride?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".