NDC 68196-140 Antibacterial Hand Sp With Light Moisturizers
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68196 - Sam's West Inc.
- 68196-140 - Antibacterial Hand Sp With Light Moisturizers
Product Packages
NDC Code 68196-140-80
Package Description: 2.36 L in 1 BOTTLE
Product Details
What is NDC 68196-140?
What are the uses for Antibacterial Hand Sp With Light Moisturizers?
Which are Antibacterial Hand Sp With Light Moisturizers 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 Sp With Light Moisturizers 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)
- LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SOY PROTEIN (UNII: R44IWB3RN5)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- NIACINAMIDE (UNII: 25X51I8RD4)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Antibacterial Hand Sp With Light Moisturizers?
- RxCUI: 995367 - triclosan 0.115 % Medicated Liquid Soap
- RxCUI: 995367 - triclosan 1.15 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".