Label: UQORA MAXIMUM UTI PAIN RELIEF- phenazopyridine hydrochloride tablet
- NDC Code(s): 73712-114-12, 73712-114-24
- Packager: Bonafide Health, LLC dba Uqora
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated October 27, 2025
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Use
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Warnings
Do not exceed recommended dosage
Do not use: if you have Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency unless approved by your physician.
Ask doctor before use if you have
■ kidney disease
■ allergies to foods, preservatives or dyes
■ had a hypersensitive reaction to phenazopyridineWhen using this product
■ stomach upset may occur, taking this product with or after meals may reduce stomach upset
■ your urine will become reddish-orange in color. This is not harmful, but care should be taken to avoid staining clothing or other items.----
■ Long-term administration of phenazopyridine hydrochloride has induced neoplasia in rats (large intestine) andmice (liver). Although no association between phenazopyridine hydrochloride and human neoplasia has beenreported, adequate epidemiological studies along these lines have not been conducted.
- Directions
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Other information
■ this product may stain contact lenses ■ this product can interfere with laboratorytests including urine, glucose (sugar), and ketones tests ■ store at room temperature 15°-30°C (59°-86°F) in adry place and protect from light ■ Tamper evident: tablets sealed in blisters. Do not use if blister foil or seal isopen or damaged
- Inactive ingredients
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PRINCIPAL DISPLAY PANEL
MAX STRENGTH MOST POWERFUL DOSE WITHOUT RX
uqora
FOUNDED BY A UTI SUFFERER
UTI PAIN RELIEF
MAX STRENGTH
FAST TARGETED RELIEF FOR
Burning
Pain & discomfort at the source unlike general pain relievers
Urgency
2 Day Supply
12 tablets
99.5 mg Phenazopyridine Hydrochloride
Not intended to replace medical care
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INGREDIENTS AND APPEARANCE
UQORA MAXIMUM UTI PAIN RELIEF
phenazopyridine hydrochloride tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73712-114 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHENAZOPYRIDINE HYDROCHLORIDE (UNII: 0EWG668W17) (PHENAZOPYRIDINE - UNII:K2J09EMJ52) PHENAZOPYRIDINE HYDROCHLORIDE 99.5 mg Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) STARCH, CORN (UNII: O8232NY3SJ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D) TALC (UNII: 7SEV7J4R1U) POVIDONE (UNII: FZ989GH94E) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) TRIACETIN (UNII: XHX3C3X673) LACTOSE (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color brown Score no score Shape OVAL Size 9mm Flavor Imprint Code p99 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73712-114-24 1 in 1 CARTON 10/27/2025 1 24 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:73712-114-12 1 in 1 CARTON 10/27/2025 2 12 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/27/2025 Labeler - Bonafide Health, LLC dba Uqora (118327455) Establishment Name Address ID/FEI Business Operations Pharbest Pharmaceuticals, Inc. 557054835 manufacture(73712-114)