NDC 62266-3245 Ho Liang Kee

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:
62266-3245
Proprietary Name:
Ho Liang Kee
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Changshu Starsea Pharmaceutical Co., Ltd.
Labeler Code:
62266
Start Marketing Date: [9]
02-23-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)

Product Packages

NDC Code 62266-3245-3

Package Description: 1 BOTTLE in 1 CARTON / 30 g in 1 BOTTLE

Product Details

What is NDC 62266-3245?

The NDC code 62266-3245 is assigned by the FDA to the product Ho Liang Kee which is product labeled by Changshu Starsea Pharmaceutical Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62266-3245-3 1 bottle in 1 carton / 30 g in 1 bottle. 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 Ho Liang Kee?

Uses for the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis & strains 

Which are Ho Liang Kee UNII Codes?

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

Which are Ho Liang Kee 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:

What is the NDC to RxNorm Crosswalk for Ho Liang Kee?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".