NDC 41520-190 Care One Antibacterial Rum Raisin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41520 - American Sales Company
- 41520-190 - Care One
Product Packages
NDC Code 41520-190-08
Package Description: 237 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 41520-190?
What are the uses for Care One Antibacterial Rum Raisin?
Which are Care One Antibacterial Rum Raisin UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Care One Antibacterial Rum Raisin 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)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- EDETATE SODIUM (UNII: MP1J8420LU)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SULISOBENZONE (UNII: 1W6L629B4K)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- CARAMEL (UNII: T9D99G2B1R)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Care One Antibacterial Rum Raisin?
- 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
* 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".