NDC 52904-794 Advil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 52904-794?
What are the uses for Advil?
Which are Advil UNII Codes?
The UNII codes for the active ingredients in this product are:
- IBUPROFEN (UNII: WK2XYI10QM)
- IBUPROFEN (UNII: WK2XYI10QM) (Active Moiety)
Which are Advil 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:
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SHELLAC (UNII: 46N107B71O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SUCROSE (UNII: C151H8M554)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WHITE WAX (UNII: 7G1J5DA97F)
- DIACETYLATED MONOGLYCERIDES (UNII: 5Z17386USF)
What is the NDC to RxNorm Crosswalk for Advil?
- RxCUI: 153008 - Advil 200 MG Oral Tablet
- RxCUI: 153008 - ibuprofen 200 MG Oral Tablet [Advil]
- 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".