NDC 58503-102 Triclosan Free Antibacterial 7.5 Oz (ocean) Antibacterial
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58503 - China Ningbo Shangge Cosmetic Technology Corp.
- 58503-102 - Triclosan Free Antibacterial 7.5 Oz (ocean)
Product Packages
NDC Code 58503-102-01
Package Description: 221 mL in 1 BOTTLE
Product Details
What is NDC 58503-102?
What are the uses for Triclosan Free Antibacterial 7.5 Oz (ocean) Antibacterial?
Which are Triclosan Free Antibacterial 7.5 Oz (ocean) 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 7.5 Oz (ocean) 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)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Triclosan Free Antibacterial 7.5 Oz (ocean) 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".