NDC 58503-100 Triclosan Free Antibacterial Antibacterial
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What is NDC 58503-100?
What are the uses for Triclosan Free Antibacterial Antibacterial?
Which are Triclosan Free Antibacterial Antibacterial UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Triclosan Free Antibacterial Antibacterial 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:
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Triclosan Free Antibacterial Antibacterial?
- RxCUI: 413261 - chloroxylenol 0.3 % Medicated Liquid Soap
- RxCUI: 413261 - chloroxylenol 3 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".