NDC 73712-500 All-in-one Uti Emergency Kit
Methenamine,Sodium Salicylate,And Phenazopyridine Hydrochloride Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BROWN (C48332)
OVAL (C48345)
9 MM
P99
Code Structure Chart
Product Details
What is NDC 73712-500?
What are the uses for All-in-one Uti Emergency Kit?
Which are All-in-one Uti Emergency Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHENAMINE (UNII: J50OIX95QV)
- METHENAMINE (UNII: J50OIX95QV) (Active Moiety)
- SODIUM SALICYLATE (UNII: WIQ1H85SYP)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- PHENAZOPYRIDINE HYDROCHLORIDE (UNII: 0EWG668W17)
- PHENAZOPYRIDINE (UNII: K2J09EMJ52) (Active Moiety)
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:
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHACRYLIC ACID-ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)
- LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for All-in-one Uti Emergency Kit?
- RxCUI: 1094147 - phenazopyridine HCl 99.5 MG Oral Tablet
- RxCUI: 1094147 - phenazopyridine hydrochloride 99.5 MG Oral Tablet
- RxCUI: 1489932 - methenamine 162 MG / sodium salicylate 162.5 MG Oral Tablet
* Please review the disclaimer below.
[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 ("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".