NDC 69729-142 Coldtac Ultra

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:
69729-142
Proprietary Name:
Coldtac Ultra
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Opmx Llc
Labeler Code:
69729
Start Marketing Date: [9]
01-05-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
11 MM
Score:
1

Product Packages

NDC Code 69729-142-06

Package Description: 3 POUCH in 1 PACKAGE / 2 TABLET in 1 POUCH

NDC Code 69729-142-72

Package Description: 72 POUCH in 1 PACKAGE / 2 TABLET in 1 POUCH

Product Details

What is NDC 69729-142?

The NDC code 69729-142 is assigned by the FDA to the product Coldtac Ultra which is product labeled by Opmx Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69729-142-06 3 pouch in 1 package / 2 tablet in 1 pouch, 69729-142-72 72 pouch in 1 package / 2 tablet 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 Coldtac Ultra?

Adults and children 12 years and over:take 2 tablets every 4-6 hoursswallow whole - do not crush, chew or dissolvedo not take more than 12 tablets in 24 hoursChildren under 12 years: ask a doctor

Which are Coldtac Ultra UNII Codes?

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

Which are Coldtac Ultra 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 Coldtac Ultra?

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: 1046781 - acetaminophen 325 MG / chlorpheniramine maleate 2 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1046781 - acetaminophen 325 MG / chlorpheniramine maleate 2 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1046781 - APAP 325 MG / chlorpheniramine maleate 2 MG / phenylephrine hydrochloride 5 MG Oral Tablet

* 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".