NDC 66949-210 Zep Professional Healthcare Worker
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66949 - Zep Inc.
- 66949-210 - Zep Professional Healthcare Worker
Product Packages
NDC Code 66949-210-01
Package Description: 1000 mL in 1 BOTTLE, PLASTIC
NDC Code 66949-210-21
Package Description: 3785 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 66949-210?
What are the uses for Zep Professional Healthcare Worker?
Which are Zep Professional Healthcare Worker UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Zep Professional Healthcare Worker 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)
- SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- SODIUM COCOYL SARCOSINATE (UNII: 1R9DUY89CZ)
- COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
- GLYCERIN (UNII: PDC6A3C0OX)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- PEG-75 LANOLIN (UNII: 09179OX7TB)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- GLUTARAL (UNII: T3C89M417N)
What is the NDC to RxNorm Crosswalk for Zep Professional Healthcare Worker?
- RxCUI: 1039078 - triclosan 0.1 % Medicated Liquid Soap
- RxCUI: 1039078 - triclosan 1 MG/ML Medicated Liquid Soap
* Please review the disclaimer below.
[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".