NDC 49035-138 Equate Maximum Strength Urinary Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
49035-138
Proprietary Name:
Equate Maximum Strength Urinary Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walmart
Labeler Code:
49035
Start Marketing Date: [9]
01-15-2015
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)
Shape:
ROUND (C48348)
Size(s):
7 MM
Imprint(s):
P97
Score:
1

Product Packages

NDC Code 49035-138-24

Package Description: 2 BLISTER PACK in 1 CARTON / 12 TABLET in 1 BLISTER PACK

Product Details

What is NDC 49035-138?

The NDC code 49035-138 is assigned by the FDA to the product Equate Maximum Strength Urinary Pain Relief which is product labeled by Walmart. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49035-138-24 2 blister pack in 1 carton / 12 tablet in 1 blister pack. 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 Equate Maximum Strength Urinary Pain Relief?

■ adults and children 12 years and over:take 2 tablets 3 times daily with a full glass of water, with or after meals as needed■ children under 12 years: consult a doctor■ Do not use for more than 2 days (12 tablets) without consulting a doctor

Which are Equate Maximum Strength Urinary Pain Relief UNII Codes?

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

  • PHENAZOPYRIDINE HYDROCHLORIDE (UNII: 0EWG668W17)
  • PHENAZOPYRIDINE (UNII: K2J09EMJ52) (Active Moiety)

Which are Equate Maximum Strength Urinary Pain Relief 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 Equate Maximum Strength Urinary Pain Relief?

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.

Patient Education

Phenazopyridine


Phenazopyridine relieves urinary tract pain, burning, irritation, and discomfort, as well as urgent and frequent urination caused by urinary tract infections, surgery, injury, or examination procedures. However, phenazopyridine is not an antibiotic; it does not cure infections.
[Learn More]


* Please review the disclaimer below.

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".