NDC 75018-004 T-dol Jiang Suan Bao

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
75018-004
Proprietary Name:
T-dol Jiang Suan Bao
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shenzhen Hanyuanhe Cultural Health Industry Development Co., Ltd.
Labeler Code:
75018
Start Marketing Date: [9]
10-10-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 75018-004-01

Package Description: 5 g in 1 POUCH

Product Details

What is NDC 75018-004?

The NDC code 75018-004 is assigned by the FDA to the product T-dol Jiang Suan Bao which is product labeled by Shenzhen Hanyuanhe Cultural Health Industry Development Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75018-004-01 5 g in 1 pouch . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for T-dol Jiang Suan Bao?

Add 150ml of water at room temperature every time, shake it and use it.

Which are T-dol Jiang Suan Bao UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are T-dol Jiang Suan Bao Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".