Label: GOUT RELIEF 3310-S- medicago sativa whole chicory root capsule
- NDC Code(s): 85631-006-01
- Packager: Bispit Canada Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated September 1, 2025
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
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- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- OTHER SAFETY INFORMATION
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WARNINGS
For your health, please read the followingcarefully
1. The use of three vials can effectivety dissolve crystallization (ittakes time to dissolve crystallization);2. The product has great somatosensation after taking it atleast 21 days in the early stage;3. Elevated uric acid or gout recurrence and site changes arenormal in the early stage of taking this product;4. Try not to drink alcohol or drink less 15 days before takingthis product;
5. This product certainly has significant effect on gout,crystallization and hyperuricemia; - PURPOSE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GOUT RELIEF 3310-S
medicago sativa whole chicory root capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:85631-006 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COIX LACRYMA-JOBI SEED (UNII: 4Q4V6NTZ1F) (COIX LACRYMA-JOBI SEED - UNII:4Q4V6NTZ1F) COIX LACRYMA-JOBI SEED 104 mg in 1.3 g MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD) (MEDICAGO SATIVA WHOLE - UNII:DJO934BRBD) MEDICAGO SATIVA WHOLE 260 mg in 1.3 g BUCKWHEAT (UNII: N0Y68724R3) (BUCKWHEAT - UNII:N0Y68724R3) BUCKWHEAT 91 mg in 1.3 g TEA LEAF (UNII: GH42T47V24) (TEA LEAF - UNII:GH42T47V24) TEA LEAF 65 mg in 1.3 g MORUS ALBA LEAF (UNII: M8YIA49Q2P) (MORUS ALBA LEAF - UNII:M8YIA49Q2P) MORUS ALBA LEAF 169 mg in 1.3 g CHICORY ROOT (UNII: 090CTY533N) (CHICORY ROOT - UNII:090CTY533N) CHICORY ROOT 299 mg in 1.3 g FU LING (UNII: XH37TWY5O4) (FU LING - UNII:XH37TWY5O4) FU LING 26 mg in 1.3 g GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY) (GLUCOSAMINE - UNII:N08U5BOQ1K) GLUCOSAMINE HYDROCHLORIDE 130 mg in 1.3 g LICORICE (UNII: 61ZBX54883) (LICORICE - UNII:61ZBX54883) LICORICE 2.6 mg in 1.3 g Inactive Ingredients Ingredient Name Strength MALTOSYL-ISOMALTOTETRAOSE (UNII: B9HR7A9UFR) SODIUM CHLORIDE (UNII: 451W47IQ8X) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) Product Characteristics Color white Score score with uneven pieces Shape CAPSULE Size 20mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:85631-006-01 60 in 1 BOTTLE 09/01/2025 1 1.3 g in 1 CAPSULE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/01/2025 Labeler - Bispit Canada Ltd. (243332192) Registrant - Bispit Canada Ltd. (243332192)
