NDC 61139-511 Highmark Professional Antibacterial Foam Handwash
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 61139-511?
What are the uses for Highmark Professional Antibacterial Foam Handwash?
Which are Highmark Professional Antibacterial Foam Handwash UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Highmark Professional Antibacterial Foam Handwash 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- LACTIC ACID (UNII: 33X04XA5AT)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- JOJOBA OIL (UNII: 724GKU717M)
- EDETATE SODIUM (UNII: MP1J8420LU)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- CORN OIL (UNII: 8470G57WFM)
- AMMONIUM SULFATE (UNII: SU46BAM238)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
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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".