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  4. NDC Product Code: 11523-4765 Coricidin Hbp Day And Night

NDC 11523-4765 Coricidin Hbp Day And Night

Dextromethorphan Hydrobromide,Guaifenesin,Acetaminophen,Chlorpheniramine Maleate Kit - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 11523-4765?
  5. Coricidin Hbp Day And Night Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

NDC Product Code:
11523-4765
Proprietary Name:
Coricidin Hbp Day And Night
Non-Proprietary Name: [1]
Dextromethorphan Hydrobromide, Guaifenesin, Acetaminophen, Chlorpheniramine Maleate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Bayer Healthcare Llc.
Labeler Code:
11523
Product Label ID:
e33f2319-2181-46db-a094-3e874b324c0a
FDA Application Number: [6]
M012
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
08-28-2009
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
Shape:
OVAL (C48345)
Size(s):
20 MM
18 MM
Imprint(s):
C;DAY
C;NIGHT
Score:
1

Product Packages

NDC Code 11523-4765-1

Package Description: 1 KIT in 1 CARTON * 2 BLISTER PACK in 1 CARTON (11523-4221-1) / 8 CAPSULE, GELATIN COATED in 1 BLISTER PACK * 2 BLISTER PACK in 1 CARTON (11523-4111-1) / 4 TABLET in 1 BLISTER PACK

Product Details

What is NDC 11523-4765?

The NDC code 11523-4765 is assigned by the FDA to the product Coricidin Hbp Day And Night which is a human over the counter drug product labeled by Bayer Healthcare Llc.. The generic name of Coricidin Hbp Day And Night is dextromethorphan hydrobromide, guaifenesin, acetaminophen, chlorpheniramine maleate. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 11523-4765-1 1 kit in 1 carton * 2 blister pack in 1 carton (11523-4221-1) / 8 capsule, gelatin coated in 1 blister pack * 2 blister pack in 1 carton (11523-4111-1) / 4 tablet in 1 blister pack. 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 Coricidin Hbp Day And Night?

Do not exceed recommended dosedo not take the Day and Night products at the same time; wait 4 hours after the last Night dose before starting Day productadults and children 12 years and over: 1 or 2 softgels every 4 hours, not more than 6 softgels in 12 hourschildren under 12 years of age: ask a doctor do not use more than directed (see overdose warning) do not take the Day and Night products at the same time; wait 4 hours after the last Day dose before starting Night productadults and children 12 years and over: 2 tablets at bedtime and every 6 hours if needed, while symptoms persist, not more than 4 tablets in a 12 hour periodchildren under 12 years of age: ask a doctor

Which are Coricidin Hbp Day And Night UNII Codes?

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

Which are Coricidin Hbp Day And Night 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 Coricidin Hbp Day And Night?

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: 1098496 - acetaminophen 500 MG / chlorpheniramine maleate 2 MG / dextromethorphan HBr 15 MG Oral Tablet
  • RxCUI: 1098496 - acetaminophen 500 MG / chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 15 MG Oral Tablet
  • RxCUI: 1098496 - APAP 500 MG / chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 15 MG Oral Tablet
  • RxCUI: 1111663 - dextromethorphan HBr 10 MG / guaiFENesin 200 MG Oral Capsule
  • RxCUI: 1111663 - dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG Oral Capsule

* Please review the disclaimer below.

Patient Education

Acetaminophen


Acetaminophen is used to relieve mild to moderate pain from headaches, muscle aches, menstrual periods, colds and sore throats, toothaches, backaches, and reactions to vaccinations (shots), and to reduce fever. Acetaminophen may also be used to relieve the pain of osteoarthritis (arthritis caused by the breakdown of the lining of the joints). Acetaminophen is in a class of medications called analgesics (pain relievers) and antipyretics (fever reducers). It works by changing the way the body senses pain and by cooling the body.
[Learn More]


Chlorpheniramine


Chlorpheniramine relieves red, itchy, watery eyes; sneezing; itchy nose or throat; and runny nose caused by allergies, hay fever, and the common cold. Chlorpheniramine helps control the symptoms of cold or allergies but will not treat the cause of the symptoms or speed recovery. Chlorpheniramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
[Learn More]


Dextromethorphan


Dextromethorphan is used to temporarily relieve cough caused by the common cold, the flu, or other conditions. Dextromethorphan will relieve a cough but will not treat the cause of the cough or speed recovery. Dextromethorphan is in a class of medications called antitussives. It works by decreasing activity in the part of the brain that causes coughing.
[Learn More]


Guaifenesin


Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a class of medications called expectorants. It works by thinning the mucus in the air passages to make it easier to cough up the mucus and clear the airways.
[Learn More]


* Please review the disclaimer below.

Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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".