NDC 63148-107 Aurora Antibacterial Vanilla Brown Sugar
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63148 - Apollo Health And Beauty Care
- 63148-107 - Aurora
Product Packages
NDC Code 63148-107-08
Package Description: 237 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 63148-107?
What are the uses for Aurora Antibacterial Vanilla Brown Sugar?
Which are Aurora Antibacterial Vanilla Brown Sugar UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Aurora Antibacterial Vanilla Brown Sugar 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)
- PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- SULISOBENZONE (UNII: 1W6L629B4K)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- VANILLA (UNII: Q74T35078H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Aurora Antibacterial Vanilla Brown Sugar?
- 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".