NDC 0573-0199 Advil Sinus Congestion And Pain
Ibuprofen,Phenylephrine Hydrochloride Tablet, Coated Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0573 - Haleon Us Holdings Llc
- 0573-0199 - Advil Sinus Congestion And Pain
Product Characteristics
Product Packages
NDC Code 0573-0199-01
Package Description: 50 POUCH in 1 TRAY / 1 TABLET, COATED in 1 POUCH
NDC Code 0573-0199-03
Package Description: 3000 POUCH in 1 CARTON / 1 TABLET, COATED in 1 POUCH
NDC Code 0573-0199-11
Package Description: 10 BLISTER PACK in 1 CARTON / 1 TABLET, COATED in 1 BLISTER PACK
NDC Code 0573-0199-21
Package Description: 20 BLISTER PACK in 1 CARTON / 1 TABLET, COATED in 1 BLISTER PACK
NDC Code 0573-0199-22
Package Description: 30 BLISTER PACK in 1 CARTON / 1 TABLET, COATED in 1 BLISTER PACK
Product Details
What is NDC 0573-0199?
What are the uses for Advil Sinus Congestion And Pain?
What are Advil Sinus Congestion And Pain Active Ingredients?
- IBUPROFEN 200 mg/1 - A non-steroidal anti-inflammatory agent with analgesic, antipyretic, and anti-inflammatory properties
- PHENYLEPHRINE HYDROCHLORIDE 10 mg/1 - An alpha-1 adrenergic agonist used as a mydriatic, nasal decongestant, and cardiotonic agent.
Which are Advil Sinus Congestion And Pain UNII Codes?
The UNII codes for the active ingredients in this product are:
- IBUPROFEN (UNII: WK2XYI10QM)
- IBUPROFEN (UNII: WK2XYI10QM) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
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:
- ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Advil Sinus Congestion And Pain?
- RxCUI: 1369775 - ibuprofen 200 MG / phenylephrine HCl 10 MG Oral Tablet
- RxCUI: 1369775 - ibuprofen 200 MG / phenylephrine hydrochloride 10 MG Oral Tablet
Which are the Pharmacologic Classes for Advil Sinus Congestion And Pain?
- Adrenergic alpha1-Agonists - [MoA] (Mechanism of Action)
- Anti-Inflammatory Agents, Non-Steroidal - [CS]
- Cyclooxygenase Inhibitors - [MoA] (Mechanism of Action)
- Nonsteroidal Anti-inflammatory Drug - [EPC] (Established Pharmacologic Class)
- alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
* 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.
[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.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[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".