NDC 42469-3001 Green Body

  1. Labeler Index
  2. Evercarepharm Co., Ltd
  3. NDC: 42469-3001 Green Body

NDC Product Code 42469-3001

NDC CODE: 42469-3001

Proprietary Name: Green Body 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: 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.

NDC Code Structure

  • 42469 - Evercarepharm Co., Ltd

NDC 42469-3001-1

Package Description: 90 TABLET in 1 CARTON

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Green Body with NDC 42469-3001 is a product labeled by Evercarepharm Co., Ltd. The generic name of Green Body is . The product's dosage form is and is administered via form.

Labeler Name: Evercarepharm Co., Ltd

Dosage Form: -

Product Type: 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.

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.
  • AMINO ACIDS, SILK (UNII: V0L00EX1IA)
  • OPHIOPOGON JAPONICUS ROOT (UNII: 90PS6JV9GZ)
  • PHELLINUS LINTEUS MYCELIUM (UNII: 40K19XJV3C)
  • EUONYMUS ALATUS WHOLE (UNII: I7IV43233H)
  • VISCUM ALBUM WHOLE (UNII: E6839Q6DO1)

Product Labeler Information

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

Labeler Name: Evercarepharm Co., Ltd
Labeler Code: 42469
Start Marketing Date: 07-03-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: I 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Green Body Product Label Images

Green Body 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

Otc - Active Ingredient

Active ingredient: maclura tricuspidata whole

Inactive Ingredient

Inactive ingredient: bombysis corpus, liriopis tuber, phellinus linteus, euonymus alatus, visci herba

Otc - Purpose

Helpful for returning functions of diabetes, pancreas and preventing and curing the complications of diabetes

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Take 3 times a day after meals with warm water

Warnings

Keep in a dry, cool placekeep away from direct sunlight

Dosage & Administration

Do not take if you are pregnant

* Please review the disclaimer below.