NDC 41520-171 Antibacterial Foaming Berry Medley
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41520 - American Sales Company
- 41520-171 - Antibacterial Foaming
Product Packages
NDC Code 41520-171-08
Package Description: 236 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 41520-171?
What are the uses for Antibacterial Foaming Berry Medley?
Which are Antibacterial Foaming Berry Medley UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Antibacterial Foaming Berry Medley 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)
- GLYCERETH-26 (UNII: NNE56F2N14)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PANTHENOL (UNII: WV9CM0O67Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SULISOBENZONE (UNII: 1W6L629B4K)
- IMIDUREA (UNII: M629807ATL)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
- GLYCERYL COCOATE (UNII: WVK1CT5994)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Antibacterial Foaming Berry Medley?
- 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".