NDC 37808-182 Cactus Flower And Mango Antibacterial Gentle Foaming Hand Sp
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What is NDC 37808-182?
What are the uses for Cactus Flower And Mango Antibacterial Gentle Foaming Hand Sp?
Which are Cactus Flower And Mango Antibacterial Gentle Foaming Hand Sp UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Cactus Flower And Mango Antibacterial Gentle Foaming Hand Sp 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)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERYL COCOATE (UNII: WVK1CT5994)
- GUAR GUM (UNII: E89I1637KE)
- EDETATE SODIUM (UNII: MP1J8420LU)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- TRIETHYLENE GLYCOL (UNII: 3P5SU53360)
- POLIDOCANOL (UNII: 0AWH8BFG9A)
- SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR)
- MANGO (UNII: I629I3NR86)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SULISOBENZONE (UNII: 1W6L629B4K)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Cactus Flower And Mango Antibacterial Gentle Foaming Hand Sp?
- RxCUI: 260054 - triclosan 0.3 % Medicated Liquid Soap
- RxCUI: 260054 - triclosan 3 MG/ML Medicated Liquid Soap
- RxCUI: 260054 - triclosan 0.3 % Foaming Medicated Hand 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".