NDC 41520-281 Antibacterial
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41520 - American Sales Company
- 41520-281 - Antibacterial
Product Packages
NDC Code 41520-281-08
Package Description: 236 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 41520-281?
What are the uses for Antibacterial?
Which are Antibacterial UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Antibacterial 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)
- CRANBERRY (UNII: 0MVO31Q3QS)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- BETAINE (UNII: 3SCV180C9W)
- SORBITOL (UNII: 506T60A25R)
- GLYCINE (UNII: TE7660XO1C)
- ALANINE (UNII: OF5P57N2ZX)
- PROLINE (UNII: 9DLQ4CIU6V)
- SERINE (UNII: 452VLY9402)
- THREONINE (UNII: 2ZD004190S)
- ARGININE (UNII: 94ZLA3W45F)
- LYSINE (UNII: K3Z4F929H6)
- GLUTAMIC ACID (UNII: 3KX376GY7L)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- POMEGRANATE (UNII: 56687D1Z4D)
What is the NDC to RxNorm Crosswalk for Antibacterial?
- RxCUI: 1020118 - triclosan 0.15 % Medicated Liquid Soap
- RxCUI: 1020118 - triclosan 1.5 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".