NDC 54340-802 Dial White Tea And Vitamin E Antibacterial Hand Soap
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What is NDC 54340-802?
What are the uses for Dial White Tea And Vitamin E Antibacterial Hand Soap?
Which are Dial White Tea And Vitamin E Antibacterial Hand Soap UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Dial White Tea And Vitamin E Antibacterial Hand Soap 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)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
- POLYETHYLENE GLYCOL 900 (UNII: UEP843BRCQ)
- GLYCERYL MONOOLEATE (UNII: 4PC054V79P)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ACETATE ION (UNII: 569DQM74SC)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
What is the NDC to RxNorm Crosswalk for Dial White Tea And Vitamin E Antibacterial Hand Soap?
- RxCUI: 1020118 - triclosan 0.15 % Medicated Liquid Soap
- RxCUI: 1020118 - triclosan 1.5 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".