13411-873 NDC - JBA GOUTAMIN (ATRACTYLODES MACROCEPHALA ,CARICA PAPAYA,CURCUMA LONGA,FIBRAUREA TINCTORIA,PERILLA FRUTESCENS,PORIA COCOS,PIPER LOLOT,ZINGIBER OFFICINALE,SIEGESBECKIA ORIENTALIS)

Drug Information

  • Product NDC: 13411-873
  • Proprietary Name: JBA Goutamin
  • Non Proprietary Name: Atractylodes macrocephala ,Carica papaya,Curcuma longa,Fibraurea tinctoria,Perilla frutescens,Poria cocos,Piper lolot,Zingiber officinale,Siegesbeckia orientalis
  • Active Ingredient(s): 116 mg/1 ATRACTYLODES MACROCEPHALA ROOT; 116 mg/1 CARICA PAPAYA WHOLE; 116 mg/1 FIBRAUREA TINCTORIA WHOLE; 116 mg/1 PERILLA FRUTESCENS WHOLE; 116 mg/1 PIPER SARMENTOSUM WHOLE; 140 mg/1 SIGESBECKIA ORIENTALIS WHOLE; 94 mg/1 TURMERIC; 116 mg/1 WOLFIPORIA COCOS WHOLE; 70 mg/1 ZINGIBER OFFICINALE WHOLE
  • Administration Route(s): ORAL
  • Dosage Form(s): TABLET

Labeler Information

Field Name Field Value
Labeler Name: Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:4/9/2025

Package Information

No. Package Code Package Description Billing Unit
113411-873-1515 TABLET in 1 BOTTLE (13411-873-15)
213411-873-3030 TABLET in 1 BOTTLE (13411-873-30)
313411-873-6060 TABLET in 1 BOTTLE (13411-873-60)

NDC Record

Field Name Field Value Definition
PRODUCT NDC13411-873The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEJBA GoutaminThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAtractylodes macrocephala ,Carica papaya,Curcuma longa,Fibraurea tinctoria,Perilla frutescens,Poria cocos,Piper lolot,Zingiber officinale,Siegesbeckia orientalisThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLETThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE4/9/2025This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEAdvanced Pharmaceutical Services, Inc. Dba Affordable Quality PharmaceuticalsName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEATRACTYLODES MACROCEPHALA ROOT; CARICA PAPAYA WHOLE; FIBRAUREA TINCTORIA WHOLE; PERILLA FRUTESCENS WHOLE; PIPER SARMENTOSUM WHOLE; SIGESBECKIA ORIENTALIS WHOLE; TURMERIC; WOLFIPORIA COCOS WHOLE; ZINGIBER OFFICINALE WHOLEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH116; 116; 116; 116; 116; 140; 94; 116; 70 
ACTIVE INGRED UNITmg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 

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This page was last updated on: 3/6/2026

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