NDC 69729-142 Coldtac Ultra
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69729 - Opmx Llc
- 69729-142 - Coldtac Ultra
Product Characteristics
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?
What are the uses for Coldtac Ultra?
Which are Coldtac Ultra UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z)
- CHLORPHENIRAMINE (UNII: 3U6IO1965U) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
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:
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STARCH, CORN (UNII: O8232NY3SJ)
- POVIDONE (UNII: FZ989GH94E)
What is the NDC to RxNorm Crosswalk for Coldtac Ultra?
- 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.
[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".