Gout Relief 3310A Plus

FDA Drug Profile — Gout Relief 3310A Plus

Gout Relief 3310A Plus is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Gout Relief 3310A Plus. Available dosage form: tablet.

Drug Details

Generic Name
Gout Relief 3310A Plus
Brand Names
Gout Relief 3310A Plus
Application Number
Sponsor
Bispit Canada Ltd.
NDC Codes
1
Dosage Forms
TABLET
Routes
ORAL
Active Ingredients
LICORICE, MEDICAGO SATIVA WHOLE, BUCKWHEAT, FU LING, CHICORY ROOT, MORUS ALBA LEAF, ANSERINE, TEA LEAF, COIX LACRYMA-JOBI SEED, GLUCOSAMINE HYDROCHLORIDE

Indications and Usage

Applicable Population:patient with gout,high uric acid, depositionof urate crystal, kidney stone and bladder stone.

Warnings

Ulsing three bottles is generally effective fordissolving crystals (as crystal dissoiution takestime); You should experience noticeable effects afterat least 21 days of conbnlous use,It is noral to experence increose in uric acidlevels or gout recurrencelchanges imn affectedareas during the early days of use;Refrain from olcohol consumption, or limit itsionificantly, for at least 15 days before takingthis product; lt has an auxiliary effect on improving libidoand supporting prostate health, Do not use if you have a seafood allergy. Store properly and out of reach of children.