NDC 77249-107 Ultima Det Antiseptic
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What is NDC 77249-107?
Which are Ultima Det Antiseptic UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Ultima Det Antiseptic 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:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- CASTOR OIL (UNII: D5340Y2I9G)
- WHITE PINE OIL (UNII: HA5CX6676U)
- LAURYL ALCOHOL (UNII: 178A96NLP2)
- S-METHYL METHANETHIOSULFONATE (UNII: 0906Z2356U)
- WATER (UNII: 059QF0KO0R)
- CARAMEL (UNII: T9D99G2B1R)
What is the NDC to RxNorm Crosswalk for Ultima Det Antiseptic?
- RxCUI: 436367 - chloroxylenol 0.5 % Medicated Liquid Soap
- RxCUI: 436367 - chloroxylenol 5 MG/ML Medicated Liquid Soap
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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".