NDC 72571-0231 Ari S-liner

Garcinia Cambogia Extract Pwd

NDC Product Code 72571-0231

NDC CODE: 72571-0231

Proprietary Name: Ari S-liner What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Garcinia Cambogia Extract Pwd What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Product Characteristics

BLACK (C48323)
Shape: ROUND (C48348)
8 MM
Score: 1
GINGER (C100097)

NDC Code Structure

  • 72571 - Ari Biotechnology Co., Ltd

NDC 72571-0231-2

Package Description: 5 g in 1 POUCH

NDC Product Information

Ari S-liner with NDC 72571-0231 is a a human over the counter drug product labeled by Ari Biotechnology Co., Ltd. The generic name of Ari S-liner is garcinia cambogia extract pwd. The product's dosage form is tablet, chewable and is administered via oral form.

Labeler Name: Ari Biotechnology Co., Ltd

Dosage Form: Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.

Product Type: Human Otc Drug What kind of product is this?
Indicates 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.

Ari S-liner Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • RICE BRAN 1.8 g/100g
  • AMINO ACIDS .2 g/100g

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.


Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Ari Biotechnology Co., Ltd
Labeler Code: 72571
Marketing Category: UNAPPROVED DRUG OTHER - What is the Marketing Category?
Product 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.

Start Marketing Date: 03-01-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 02-28-2022 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Ari S-liner Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Indications & Usage

Fluids metabolism smoothBlood metabolism smoothReducing body fatElimination of waste in bloodRemove swellingAcquiring gastrointestinal satisfactionReducing food intake

Otc - Keep Out Of Reach Of Children


These Highlights Do Not Include All The Information Needed To Use. See Full Prescribing Information.

Serving Size: 1 pouch (5g)Serving Per Container: 90Serving size 1 pouch, 3-times a day1 Month Supply, 90 pouches


Warning: Individuals 15 years and older, take 3 packets daily per serving with water. Children 3-15 years may take half the adult serving.

Otc - Purpose

Reduces obesity

Inactive Ingredient

Inactive ingredients:Coix Pwd - 35.3%The Foxglove Pwd - 10.7%Longan Pwd - 8.5%Chinese dioscorea Pwd - 7.7%Chinese matrimony vine pwd - 5.2%Morus bark pwd - 5.2%Milk Vetch Root pwd - 5.2%Alisma Pwd - 5.2%Amomum seed pwd - 3.8%Cnidium Pwd - 3.2%Liquorice Pwd - 3.2%

Otc - Active Ingredient

Active IngredientsGarciniaCambogia Extract pwd - 6.8%Rice Bran - 1.8%Amino Acids - 0.2%

Recent Major Changes

90 pouches : 1 pouch (5g) x 90

Address 6F, Ari Bldg., 411, Eonju-ro, Gangnam-gu, Seoul, Korea

Address 3F, Ari Bldg., 411, Eonju-ro, Gangnam-gu, Seoul, Korea

Supplement Facts

Serving Size : 1 pouch (5g) / Serving Per Container : 90

* Please review the disclaimer below.