NDC 68196-143 Antibacterial Light Moisturizers Refill
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68196 - Sam's West Inc.
- 68196-143 - Antibacterial
Product Packages
NDC Code 68196-143-80
Package Description: 2.36 L in 1 BOTTLE
Product Details
What is NDC 68196-143?
What are the uses for Antibacterial Light Moisturizers Refill?
Which are Antibacterial 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 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 Light Moisturizers Refill?
- 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".