NDC 63868-453 Ibuprofen And Pseudoephedrine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63868 - Chain Drug Marketing Association Inc.
- 63868-453 - Ibuprofen And Pseudoephedrine Hydrochloride
Product Characteristics
Product Packages
NDC Code 63868-453-20
Package Description: 20 TABLET, SUGAR COATED in 1 BLISTER PACK
Price per Unit: $0.17314 per EA
Product Details
What is NDC 63868-453?
What are the uses for Ibuprofen And Pseudoephedrine Hydrochloride?
Which are Ibuprofen And Pseudoephedrine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- IBUPROFEN (UNII: WK2XYI10QM)
- IBUPROFEN (UNII: WK2XYI10QM) (Active Moiety)
- PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N)
- PSEUDOEPHEDRINE (UNII: 7CUC9DDI9F) (Active Moiety)
Which are Ibuprofen And Pseudoephedrine Hydrochloride 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:
- ACACIA (UNII: 5C5403N26O)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- STARCH, CORN (UNII: O8232NY3SJ)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- CROSPOVIDONE (UNII: 68401960MK)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- GELATIN (UNII: 2G86QN327L)
- GUAR GUM (UNII: E89I1637KE)
- TRISTEARIN (UNII: P6OCJ2551R)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- KAOLIN (UNII: 24H4NWX5CO)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- POVIDONE (UNII: FZ989GH94E)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WHITE WAX (UNII: 7G1J5DA97F)
What is the NDC to RxNorm Crosswalk for Ibuprofen And Pseudoephedrine Hydrochloride?
- RxCUI: 1299021 - ibuprofen 200 MG / pseudoephedrine HCl 30 MG Oral Tablet
- RxCUI: 1299021 - ibuprofen 200 MG / pseudoephedrine hydrochloride 30 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.
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Pseudoephedrine
Pseudoephedrine is used to relieve nasal congestion caused by colds, allergies, and hay fever. It is also used to temporarily relieve sinus congestion and pressure. Pseudoephedrine will relieve symptoms but will not treat the cause of the symptoms or speed recovery. Pseudoephedrine is in a class of medications called nasal decongestants. It works by causing narrowing of the blood vessels in the nasal passages.
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* 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".