FDA Label for Gout Relief 3310a Plus
View Indications, Usage & Precautions
Gout Relief 3310a Plus Product Label
The following document was submitted to the FDA by the labeler of this product Bispit Canada Ltd.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
MEDICAGO SATIVA WHOLE
CHICORY ROOT
GLUCOSAMINE HYDROCHLORIDE
BUCKWHEAT
TEA LEAF
MORUS ALBA LEAF
LICORICE
FU LING
COIX LACRYMA-JOBI SEED
ANSERINE
Inactive Ingredient
CALCIUM CARBONATE
SODIUM CHLORIDE
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.
Otc - Keep Out Of Reach Of Children
Store properly and out of reach of children.
Otc - Purpose
This product is a pure plant extract; it canreduce the frequency of goutattacks; dissolve the crystals in thejoints; promote the excretion of blood uricacids,andimprove the purine metabolismand excretory system.
Dosage & Administration
2 tablets in the momingand 2 toblets in the evening.
Indications & Usage
Applicable Population:patient with gout,high uric acid, depositionof urate crystal, kidney stone and bladder
stone.
Package Label.Principal Display Panel
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