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NDC 73712-500 All-in-one Uti Emergency Kit

Methenamine,Sodium Salicylate,And Phenazopyridine Hydrochloride Kit - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 73712-500?
  5. All-in-one Uti Emergency Kit Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

Get all the details for National Drug Code (NDC) 73712-500 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
73712-500
Proprietary Name:
All-in-one Uti Emergency Kit
Non-Proprietary Name: [1]
Methenamine, Sodium Salicylate, And Phenazopyridine Hydrochloride
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Uqora Inc
Labeler Code:
73712
Product Label ID:
ebde96d2-e1f2-26b1-e053-2a95a90a2fb1
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date: [9]
10-17-2022
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

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 73712-500?

The NDC code 73712-500 is assigned by the FDA to the product All-in-one Uti Emergency Kit which is a human over the counter drug product labeled by Uqora Inc. The generic name of All-in-one Uti Emergency Kit is methenamine, sodium salicylate, and phenazopyridine hydrochloride. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 73712-500-24 1 kit in 1 carton * 12 tablet in 1 blister pack (73712-804-12) * 12 tablet in 1 blister pack (73712-113-12). 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 All-in-one Uti Emergency Kit?

This product is used as Active ingredients (in each tablet)PurposeMethenamine 162mgAntibacterialSodium Salicylate 162.5mg (NSAID)**nonsteroidal anti-inflammatory drugAnalgesic (pain reliever)Active ingredient (in each tablet) PurposePhenazopyridine Hydrochloride 99.5mgUrinary Tract Analgesic

Which are All-in-one Uti Emergency Kit UNII Codes?

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

Which are All-in-one Uti Emergency Kit 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 All-in-one Uti Emergency Kit?

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:

* Please review the disclaimer below.

Product Footnotes

[1] 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.

[3] 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.

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

[8] 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.

[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, 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".