NDC 70332-101 Ketophene
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70332-101?
Which are Ketophene UNII Codes?
The UNII codes for the active ingredients in this product are:
- KETOPROFEN (UNII: 90Y4QC304K)
- KETOPROFEN (UNII: 90Y4QC304K) (Active Moiety)
Which are Ketophene 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:
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- WATER (UNII: 059QF0KO0R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- SORBITOL (UNII: 506T60A25R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- EDETATE SODIUM (UNII: MP1J8420LU)
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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".