Gout Relief 3310-S
Active substance: GLUCOSAMINE HYDROCHLORIDE, MORUS ALBA LEAF, LICORICE, PUERARIN, BUCKWHEAT, SODIUM CHLORIDE, MEDICAGO SATIVA WHOLE, TEA LEAF, CELERY SEED, CHICORY ROOT
CAPSULE · GLUCOSAMINE HYDROCHLORIDE 130 mg/1.3g, MORUS ALBA LEAF 39 mg/1.3g, LICORICE 2.6 mg/1.3g, PUERARIN 65 mg/1.3g, BUCKWHEAT 91 mg/1.3g, SODIUM CHLORIDE 26 mg/1.3g, MEDICAGO SATIVA WHOLE 260 mg/1.3g, TEA LEAF 65 mg/1.3g, CELERY SEED 260 mg/1.3g, CHICORY ROOT 234 mg/1.3g
United StatesActive
Marketing holder: Bispit Canada Ltd.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
Composition
- GLUCOSAMINE HYDROCHLORIDE · 130 mg/1.3g
- MORUS ALBA LEAF · 39 mg/1.3g
- LICORICE · 2.6 mg/1.3g
- PUERARIN · 65 mg/1.3g
- BUCKWHEAT · 91 mg/1.3g
- SODIUM CHLORIDE · 26 mg/1.3g
- MEDICAGO SATIVA WHOLE · 260 mg/1.3g
- TEA LEAF · 65 mg/1.3g
- CELERY SEED · 260 mg/1.3g
- CHICORY ROOT · 234 mg/1.3g
Registration
- Registration number
- 85631-003
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 85631-003 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 85631-003 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 85631-003 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 85631-003 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 85631-003 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 85631-003 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 85631-003 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 85631-003 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 85631-003 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 85631-003 · Verified 2026-10-09 · open in source
- ingredients.8 · openFDA NDC · 85631-003 · Verified 2026-10-09 · open in source
- ingredients.9 · openFDA NDC · 85631-003 · Verified 2026-10-09 · open in source