NDC 50988-453 Shopko Antibacterial Deep Cleansing Hand
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 50988-453?
What are the uses for Shopko Antibacterial Deep Cleansing Hand?
Which are Shopko Antibacterial Deep Cleansing Hand UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Shopko Antibacterial Deep Cleansing 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- LACTOSE (UNII: J2B2A4N98G)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- HYPROMELLOSE 2208 (100 MPA.S) (UNII: B1QE5P712K)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- ULTRAMARINE BLUE (UNII: I39WR998BI)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
- SULISOBENZONE (UNII: 1W6L629B4K)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Shopko Antibacterial Deep Cleansing Hand?
- RxCUI: 413246 - triclosan 0.2 % Medicated Liquid Soap
- RxCUI: 413246 - triclosan 2 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".