NDC 54622-575 Hibiclens For Georgia Pacific
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54622 - Georgia-pacific Consumer Products Lp
- 54622-575 - Hibiclens For Georgia Pacific
Product Characteristics
Product Packages
NDC Code 54622-575-73
Package Description: 1200 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 54622-575?
What are the uses for Hibiclens For Georgia Pacific?
Which are Hibiclens For Georgia Pacific UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
- CHLORHEXIDINE (UNII: R4KO0DY52L) (Active Moiety)
Which are Hibiclens For Georgia Pacific 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:
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- WATER (UNII: 059QF0KO0R)
- POLOXAMER 237 (UNII: JT3U72U71K)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
What is the NDC to RxNorm Crosswalk for Hibiclens For Georgia Pacific?
- RxCUI: 211365 - chlorhexidine gluconate 4 % Medicated Liquid Soap
- RxCUI: 211365 - chlorhexidine gluconate 40 MG/ML Medicated Liquid Soap
- RxCUI: 211365 - chlorhexidine gluconate 4 % Medicated Surgical Scrub
- RxCUI: 834167 - HIBICLENS 4 % Medicated Liquid Soap
- RxCUI: 834167 - chlorhexidine gluconate 40 MG/ML Medicated Liquid Soap [Hibiclens]
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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".