NDC 67536-884 Quali Cold

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:
67536-884
Proprietary Name:
Quali Cold
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Teh Seng Pharmaceutical Mfg. Co., Ltd
Labeler Code:
67536
Start Marketing Date: [9]
10-10-2013
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 67536-884-01

Package Description: 100 PACKET in 1 BOX / 16 g in 1 PACKET

Product Details

What is NDC 67536-884?

The NDC code 67536-884 is assigned by the FDA to the product Quali Cold which is product labeled by Teh Seng Pharmaceutical Mfg. Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 67536-884-01 100 packet in 1 box / 16 g in 1 packet. 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 Quali Cold?

1. Clean and dry the affected areas before application.2. Remove the protective film while applying the areas 1-2 times daily, cut into smaller size if desired. If necessary up to 3 sheets per day.3. Use only as directed. Firmly affix with adhesive tapes or elastic bandages around joint areas to secure the patch if needed.

Which are Quali Cold UNII Codes?

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

Which are Quali Cold 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 Quali Cold?

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:
  • RxCUI: 1812753 - camphor 0.5 % / menthol 1 % / methyl salicylate 2 % Medicated Patch
  • RxCUI: 1812753 - camphor 0.005 MG/MG / menthol 0.01 MG/MG / methyl salicylate 0.02 MG/MG Medicated Patch

* 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".