NDC 68196-141 Antibacterial Hand Sp With Light Moisturizers Refill
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What is NDC 68196-141?
What are the uses for Antibacterial Hand Sp With Light Moisturizers Refill?
Which are Antibacterial Hand Sp With Light Moisturizers Refill 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 Refill 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)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- SOY PROTEIN (UNII: R44IWB3RN5)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .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)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Antibacterial Hand Sp With Light Moisturizers Refill?
- RxCUI: 995367 - triclosan 0.115 % Medicated Liquid Soap
- RxCUI: 995367 - triclosan 1.15 MG/ML Medicated Liquid Soap
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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".