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  4. NDC Product Code: 57708-888 Nin Jiom Pei Pa Koa

NDC 57708-888 Nin Jiom Pei Pa Koa

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 57708-888?
  5. Nin Jiom Pei Pa Koa 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:
57708-888
Proprietary Name:
Nin Jiom Pei Pa Koa
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nin Jiom Medicine Manufactory (hk) Ltd
Labeler Code:
57708
Product Label ID:
ad386748-3cbe-4d2f-972d-2ccf1b04aaac
Start Marketing Date: [9]
09-01-2006
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BLACK (C48323)
Flavor(s):
HONEY (C73394 - HERBAL HONEY LOQUAT FLAVORED)

Code Structure Chart

Product Details

What is NDC 57708-888?

The NDC code 57708-888 is assigned by the FDA to the product Nin Jiom Pei Pa Koa which is product labeled by Nin Jiom Medicine Manufactory (hk) Ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 57708-888-02 24 bottle, glass in 1 carton / 300 ml in 1 bottle, glass (57708-888-01), 57708-888-04 48 bottle, glass in 1 carton / 150 ml in 1 bottle, glass (57708-888-03). 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 Nin Jiom Pei Pa Koa?

For the temporary relief of minor discomfort and protection of irritated areas in sore mouth and sore throat.

Which are Nin Jiom Pei Pa Koa UNII Codes?

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

Which are Nin Jiom Pei Pa Koa 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".