NDC 44224-0018 Easy Care First Aid Ibuprofen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 44224 - Tender Corporation
- 44224-0018 - Easy Care First Aid Ibuprofen
Product Characteristics
Product Packages
NDC Code 44224-0018-1
Package Description: 2 TABLET, COATED in 1 PACKET
NDC Code 44224-0018-2
Package Description: 50 PACKET in 1 BOX / 2 TABLET, COATED in 1 PACKET
Product Details
What is NDC 44224-0018?
What are the uses for Easy Care First Aid Ibuprofen?
Which are Easy Care First Aid Ibuprofen UNII Codes?
The UNII codes for the active ingredients in this product are:
- IBUPROFEN (UNII: WK2XYI10QM)
- IBUPROFEN (UNII: WK2XYI10QM) (Active Moiety)
Which are Easy Care First Aid Ibuprofen 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POVIDONE K30 (UNII: U725QWY32X)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- TALC (UNII: 7SEV7J4R1U)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
What is the NDC to RxNorm Crosswalk for Easy Care First Aid Ibuprofen?
- RxCUI: 310965 - ibuprofen 200 MG Oral Tablet
- RxCUI: 310965 - ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral Tablet
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[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".