NDC 51811-066 Antibacterial Protective Hand
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51811 - Hanover Pen Corp Dba Hpc Global
- 51811-066 - Antibacterial Protective Hand
Product Packages
NDC Code 51811-066-99
Package Description: 14.15 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 51811-066?
What are the uses for Antibacterial Protective Hand?
Which are Antibacterial Protective Hand UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
- CHLORHEXIDINE (UNII: R4KO0DY52L) (Active Moiety)
Which are Antibacterial Protective Hand 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:
- ALOE VERA FLOWER (UNII: 575DY8C1ER)
- CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PANTHENOL (UNII: WV9CM0O67Z)
- POVIDONE K30 (UNII: U725QWY32X)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- ZINC OXIDE (UNII: SOI2LOH54Z)
What is the NDC to RxNorm Crosswalk for Antibacterial Protective Hand?
- RxCUI: 834176 - chlorhexidine gluconate 0.5 % Topical Solution
- RxCUI: 834176 - chlorhexidine gluconate 5 MG/ML Topical Solution
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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".