NDC 75018-002 T-dol Yi Dao Bao

Solid Powder

NDC Product Code 75018-002

NDC 75018-002-01

Package Description: 5 g in 1 POUCH

NDC Product Information

T-dol Yi Dao Bao with NDC 75018-002 is a a human over the counter drug product labeled by Shenzhen Hanyuanhe Cultural Health Industry Development Co., Ltd.. The generic name of T-dol Yi Dao Bao is solid powder. The product's dosage form is powder and is administered via oral form.

Labeler Name: Shenzhen Hanyuanhe Cultural Health Industry Development Co., Ltd.

Dosage Form: Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.

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.

T-dol Yi Dao Bao 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.

  • MOMORDICA CHARANTIA FRUIT 1.5 g/5g

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: Shenzhen Hanyuanhe Cultural Health Industry Development Co., Ltd.
Labeler Code: 75018
Marketing Category: UNAPPROVED HOMEOPATHIC - 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: 10-10-2019 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: 12-31-2020 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: N 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’.

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T-dol Yi Dao Bao Product Label Images