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  4. NDC Product Code: 69729-322 Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl

NDC 69729-322 Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69729-322?
  5. Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69729-322
Proprietary Name:
Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Opmx Llc
Labeler Code:
69729
Product Label ID:
b3c229a4-c772-70fb-e053-2a95a90a72db
Start Marketing Date: [9]
08-26-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
13 MM
Imprint(s):
S78
Score:
1

Code Structure Chart

Product Details

What is NDC 69729-322?

The NDC code 69729-322 is assigned by the FDA to the product Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl which is product labeled by Opmx Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 69729-322-27 2 tablet in 1 pouch , 69729-322-37 12 tablet in 1 pouch , 69729-322-38 144 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 Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl?

Temporarily relieves these symptoms of hay fever or other respiratory allergies:HeadacheNasal congestionSinus congestion & pressureRunny nose and sneezingMinor aches & painTemporarily relieves these additional symptoms of hay fever:itching of the nose or throatitchy, watery eyeshelps clear nasal passageshelps decongest sinus opening and passages

Which are Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl UNII Codes?

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

Which are Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl 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 Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl?

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: 2463332 - acetaminophen 500 MG / chlorpheniramine maleate 4 MG / phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 2463332 - acetaminophen 500 MG / chlorpheniramine maleate 4 MG / phenylephrine hydrochloride 10 MG Oral Tablet
  • RxCUI: 2463332 - APAP 500 MG / chlorpheniramine maleate 4 MG / phenylephrine hydrochloride 10 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".