JBA GOUTAMIN- atractylodes macrocephala ,carica papaya,curcuma longa,fibraurea tinctoria,perilla frutescens,poria cocos,piper lolot,zingiber officinale,siegesbeckia orientalis tablet

JBA Goutamin by

Drug Labeling and Warnings

JBA Goutamin by is a Otc medication manufactured, distributed, or labeled by Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Identity

Dietary Supplement

Direction

Adults – Take 2 tablets twice daily (morning and evening) preferably after a meal.

Safe handling warning 

GOUTAMIN
NATURAL GOUT SUPPORT*
Promotes Uric Acid Balance*
Enhances Gout Health*
GOUTAMIN supports the alleviation of gout symptoms by:
- Reducing inflammation & promoting joint health*
- Assisting in lowering uric acid levels in the body*
- Supporting healthy kidney function*
- Enhancing joint mobility and flexibility*
- Providing antioxidant benefits to fight oxidative stress*

* These statements have not been evaluated by the Food & Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

HEALTH CLAIM

PRECAUTIONS

WARNINGS

• If you are pregnant, nursing or have a medical condition, consult your physician before use.
• Do not use if tamper-evident seal is broken or missing.
• Keep Out of The Reach of Children.
• Store in a cool, dry place (59oF-86oF), avoid moisture and light.

ACTIVE INGREDIENT

PURPOSE

Other ingredients

Calcium Stearate, Colloidal Silicon Dioxide, Corn Starch, Ferric Oxides, Hydroxypropyl Methylcellulose, Microcrystalline Cellulose, Polyethylene
Glycol 6000, Polyvinylpyrrolidone (PVP), Sodium Carboxymethylcellulose, Talc, Titanium Dioxide.

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

Product label

INGREDIENTS AND APPEARANCE

JBA GOUTAMIN 
atractylodes macrocephala ,carica papaya,curcuma longa,fibraurea tinctoria,perilla frutescens,poria cocos,piper lolot,zingiber officinale,siegesbeckia orientalis tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 13411-873
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ATRACTYLODES MACROCEPHALA ROOT (UNII: 08T3N29QJB) (ATRACTYLODES MACROCEPHALA ROOT - UNII:08T3N29QJB)	ATRACTYLODES MACROCEPHALA ROOT	116 mg
CARICA PAPAYA WHOLE (UNII: S0U63B0Q51) (CARICA PAPAYA WHOLE - UNII:S0U63B0Q51)	CARICA PAPAYA WHOLE	116 mg
TURMERIC (UNII: 856YO1Z64F) (CURCUMA LONGA (TURMERIC) ROOT - UNII:856YO1Z64F)	TURMERIC	94 mg
FIBRAUREA TINCTORIA WHOLE (UNII: 2E7B273DUH) (FIBRAUREA TINCTORIA WHOLE - UNII:2E7B273DUH)	FIBRAUREA TINCTORIA WHOLE	116 mg
PERILLA FRUTESCENS WHOLE (UNII: XUR646842C) (PERILLA FRUTESCENS WHOLE - UNII:XUR646842C)	PERILLA FRUTESCENS WHOLE	116 mg
WOLFIPORIA COCOS WHOLE (UNII: Y1I7Z6FF4R) (WOLFIPORIA COCOS WHOLE - UNII:Y1I7Z6FF4R)	WOLFIPORIA COCOS WHOLE	116 mg
PIPER SARMENTOSUM WHOLE (UNII: 31807Q9AD5) (PIPER SARMENTOSUM WHOLE - UNII:31807Q9AD5)	PIPER SARMENTOSUM WHOLE	116 mg
ZINGIBER OFFICINALE WHOLE (UNII: IN6Q3S3414) (ZINGIBER OFFICINALE WHOLE - UNII:IN6Q3S3414)	ZINGIBER OFFICINALE WHOLE	70 mg
SIGESBECKIA ORIENTALIS WHOLE (UNII: ZM9Q0FEI4Z) (SIGESBECKIA ORIENTALIS WHOLE - UNII:ZM9Q0FEI4Z)	SIGESBECKIA ORIENTALIS WHOLE	140 mg

Inactive Ingredients
Ingredient Name	Strength
CALCIUM STEARATE (UNII: 776XM7047L)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STARCH, CORN (UNII: O8232NY3SJ)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
POVIDONE K30 (UNII: U725QWY32X)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	brown	Score	no score
Shape	CAPSULE	Size	22mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 13411-873-60	60 in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2025
2	NDC: 13411-873-30	30 in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2025
3	NDC: 13411-873-15	15 in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/09/2025

Labeler - Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals (187498279)

Establishment
Name	Address	ID/FEI	Business Operations
Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals		187498279	manufacture(13411-873)