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  4. NDC Product Code: 69927-004 Balmers Hanryeoncho Suseunghwa

NDC 69927-004 Balmers Hanryeoncho Suseunghwa

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69927-004?
  5. Balmers Hanryeoncho Suseunghwa Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69927-004
Proprietary Name:
Balmers Hanryeoncho Suseunghwa
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tae Eul Bi Co., Ltd.
Labeler Code:
69927
Product Label ID:
43aa5ed7-9fd7-482e-a3e5-cd4050a864dd
Start Marketing Date: [9]
07-20-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332 - BROWN)
Shape:
BULLET (C48335)
Size(s):
3 MM
Imprint(s):
3;HP;X
Score:
1

Code Structure Chart

Product Details

What is NDC 69927-004?

The NDC code 69927-004 is assigned by the FDA to the product Balmers Hanryeoncho Suseunghwa which is product labeled by Tae Eul Bi Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69927-004-01 6.5 g in 1 package . 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 Balmers Hanryeoncho Suseunghwa?

Take 2~3 packs a day with warm water regardless before/after a meal (based on one pack a time)

Which are Balmers Hanryeoncho Suseunghwa UNII Codes?

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

  • FALLOPIA MULTIFLORA ROOT (UNII: AUZ3VD75MC)
  • FALLOPIA MULTIFLORA ROOT (UNII: AUZ3VD75MC) (Active Moiety)

Which are Balmers Hanryeoncho Suseunghwa 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:

* Please review the disclaimer below.

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".