NDC 0363-0243 Antibacterial Hand
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreen Co
- 0363-0243 - Antibacterial Hand
Product Packages
NDC Code 0363-0243-81
Package Description: .332 L in 1 BOTTLE, PLASTIC
NDC Code 0363-0243-97
Package Description: 1.89 L in 1 BOTTLE, PLASTIC
Product Details
What is NDC 0363-0243?
What are the uses for Antibacterial Hand?
Which are Antibacterial Hand UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Antibacterial 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:
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG-18 GLYCERYL OLEATE/COCOATE (UNII: VD2D270332)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
What is the NDC to RxNorm Crosswalk for Antibacterial Hand?
- RxCUI: 1020118 - triclosan 0.15 % Medicated Liquid Soap
- RxCUI: 1020118 - triclosan 1.5 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".