NDC 52904-782 Advil Sinus Congestion And Pain

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:
52904-782
Proprietary Name:
Advil Sinus Congestion And Pain
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
52904
Start Marketing Date: [9]
07-01-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)
Shape:
OVAL (C48345)
Size(s):
15 MM
Imprint(s):
1200;P10
Score:
1

Code Structure Chart

Product Details

What is NDC 52904-782?

The NDC code 52904-782 is assigned by the FDA to the product Advil Sinus Congestion And Pain which is product labeled by Select Corporation. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 52904-782-03 1 pouch in 1 blister pack / 1 tablet, coated in 1 pouch, 52904-782-04 2 pouch in 1 blister pack / 1 tablet, coated in 1 pouch, 52904-782-25 25 pouch in 1 carton / 1 tablet, coated in 1 pouch, 52904-782-50 50 pouch in 1 carton / 1 tablet, coated 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 Advil Sinus Congestion And Pain?

Do not take more than directedadults and children 12 years of age and over:take 1 tablet every 4 hours while symptoms persist. do not use more than 6 tablets in any 24-hour period unless directed by a doctorchildren under 12 years of age: do not use because this product contains too much medication for children under this age

Which are Advil Sinus Congestion And Pain UNII Codes?

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

Which are Advil Sinus Congestion And Pain 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 Advil Sinus Congestion And Pain?

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: 1369775 - ibuprofen 200 MG / phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 1369775 - ibuprofen 200 MG / phenylephrine hydrochloride 10 MG Oral Tablet

* Please review the disclaimer below.

Patient Education

Ibuprofen


Prescription ibuprofen is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints) and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints). It is also used to relieve mild to moderate pain, including menstrual pain (pain that happens before or during a menstrual period). Nonprescription ibuprofen is used to reduce fever and to relieve minor aches and pain from headaches, muscle aches, arthritis, menstrual periods, the common cold, toothaches, and backaches. Ibuprofen is in a class of medications called NSAIDs. It works by stopping the body's production of a substance that causes pain, fever, and inflammation.
[Learn More]


Phenylephrine


Phenylephrine is used to relieve nasal discomfort caused by colds, allergies, and hay fever. It is also used to relieve sinus congestion and pressure. Phenylephrine will relieve symptoms but will not treat the cause of the symptoms or speed recovery. Phenylephrine is in a class of medications called nasal decongestants. It works by reducing swelling of the blood vessels in the nasal passages.
[Learn More]


* 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".