UQORA ANTIBACTERIAL PLUS URINARY PAIN RELIEF- methenamine, sodium salicylate tablet

Uqora Antibacterial Plus Urinary Pain Relief by

Drug Labeling and Warnings

Uqora Antibacterial Plus Urinary Pain Relief by is a Otc medication manufactured, distributed, or labeled by Uqora Inc, Reese Pharmaceutical Co, Pharbest. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients (in each tablet):

Methenamine 162 mg

Sodium Salicylate 162.5 mg (NSAID Nonsteroidal Anti-Inflammatory Drug)

Purpose

Antibacterial

Analgesic (pain reliever)

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

Uses Temporarily relieves: pain & burning frequency and urgency of urination

Warnings

Reye's syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. If changes in behaviour with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

Stomach bleeding warning: This product contains an NSAID, which may cause stomach bleeding. The chance is higher if you:

take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen or others)

have 3 or more alcoholic drinks every day while using this product

have stomach ulcers or bleeding problems take a blood thinning (anticoagulant) or steroid drug

are age 60 or older take more or for a longer time than directed

Do not use:

if you are on a sodium restricted diet

if you are allergic to salicylates (including aspirin) unless directed by a doctor

if you have stomach problems (such as heartburn, upset stomach, or stomach pain) that persist or recur, or if you have ulcers or bleeding problems unless directed by a doctor

Ask a doctor before use if you have

frequent, burning urination for the first time the stomach bleeding warning applying to you

history of stomach problems, such as heartburn

high blood pressure heart disease liver cirrhosis bleeding problems

diuretic use ulcers kidney disease reached age 60 or older

Ask a doctor or pharmacist before use if you are

taking any other drug containing an NSAID (prescription or nonprescription)

taking a blood thinning (anticoagulant), steroid, diabetes, gout or arthritis drug

When using this product do not take more than the recommended dosage

Stop and ask a doctor if

product has been used for 3 days

you experience any of the following signs of stomach bleeding:

feel faint, vomit blood have bloody or black stools have stomach pain that does not get better

ringing in the ears or a loss of hearing occurs

If pregnant or breast feeding, ask a health professional before use.

DOSAGE & ADMINISTRATION

Directions: Adults and children 12 years and over: take 2 tablets with a full glass of water 3 times a day. Drink plenty of fluids. Children under 12 years: ask a doctor

INACTIVE INGREDIENT

Inactive ingredients:

benzoic acid, croscarmellose sodium, fd&c red #40, fd&c yellow #6, hypromellose, magnesium stearate, methacrylic acid-ethyl acrylate copolymer, microcrystalline cellulose, silicon dioxide, stearic acid, sodium bicarbonate, sodium lauryl sulfate, talc, titanium dioxide, triacetin, triethyl citrate

STORAGE AND HANDLING

Other Information: each tablet contains 25 mg of sodium store at 59-86°F (15-30°C) in a dry place protect from light Tamper evident: tablets sealed in blisters. Do not use if blister foil or seal is open or damaged.

SPL UNCLASSIFIED SECTION

• HELPS CONTROL THE INFECTION*
• PLUS GENERAL PAIN RELIEVER

Antibacterial Urinary Pain Relief

Methenamine and Sodium Salicylate (NSAID)

Packaging

INGREDIENTS AND APPEARANCE

UQORA ANTIBACTERIAL PLUS URINARY PAIN RELIEF 
methenamine, sodium salicylate tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73712-804
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHENAMINE (UNII: J50OIX95QV) (METHENAMINE - UNII:J50OIX95QV)	METHENAMINE	162 mg
SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SODIUM SALICYLATE	162.5 mg

Inactive Ingredients
Ingredient Name	Strength
BENZOIC ACID (UNII: 8SKN0B0MIM)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
HYPROMELLOSES (UNII: 3NXW29V3WO)
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 BICARBONATE (UNII: 8MDF5V39QO)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TRIACETIN (UNII: XHX3C3X673)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)

Product Characteristics
Color	red	Score	no score
Shape	ROUND	Size	11mm
Flavor		Imprint Code	PH061
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73712-804-24	1 in 1 CARTON	04/29/2020
1		24 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		04/29/2020

Labeler - Uqora Inc (022730893)

Registrant - Reese Pharmaceutical Co (004172052)

Establishment
Name	Address	ID/FEI	Business Operations
Reese Pharmaceutical Co		004172052	repack(73712-804) , relabel(73712-804)

Establishment
Name	Address	ID/FEI	Business Operations
Pharbest		557054835	manufacture(73712-804)