Uti Emergency Relief Kit
NDC 73436-4882

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 73436-4882?
  5. Uti Emergency Relief Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

Uti Emergency Relief (methenamine, sodium salicylate, and phenazopyridine hydrochloride kit) is a UNAPPROVED DRUG OTHER-approved product labeled by Cadence Health, Inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a red kit. This product entry covers the primary NDC 73436-4882 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
73436-4882
Proprietary Name:
Uti Emergency Relief
Non-Proprietary Name: [1]
Methenamine, Sodium Salicylate, And Phenazopyridine Hydrochloride Kit
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Kit - A packaged collection of related material.

Labeler & Regulatory Data

Labeler Name: [5]
Cadence Health, Inc.
Labeler Code:
73436
Product Label ID:
3a923df5-15ed-404d-8741-33a9793cb7f5
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.

Marketing Timeline

Start Marketing Date: [9]
04-06-2026
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N

Product Characteristics

Color(s):
RED (C48326)
BROWN (C48332)
Shape:
ROUND (C48348)
OVAL (C48345)
Size(s):
11 MM
9 MM
Imprint(s):
PH061
P99
Score:
1

Code Structure Chart

Product Details

What is NDC 73436-4882?

The NDC code 73436-4882 is assigned by the FDA to the product Uti Emergency Relief. It is commonly known by its generic name, methenamine, sodium salicylate, and phenazopyridine hydrochloride kit. This pharmaceutical product is labeled by Cadence Health, Inc. and is currently categorized as listed product. The medication is a kit. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 73436-4882-4. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

UTI Infection ControlAdults and children 12 years and over:take 2 tablets with a full glass of water 3 times a day. Drink plenty of fluids.Do not use for more than a 3 day period unless directed by a doctor.Children under 12 years:ask a doctor. UTI Pain ReliefAdults and children 12 years and over:take 2 tablets 3 times daily with a full glass of water, with or after meals as neededDo not use for more than 2 days (12 tablets) without consulting a doctor.Children under 12 years: ask a doctor.

Which are the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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 this product?

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 & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What kind of product is this? Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".