NDC 51230-391 Noxicare
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51230 - Truceuticals, Llc
- 51230-391 - Noxicare
Product Characteristics
Product Packages
NDC Code 51230-391-01
Package Description: 1 TUBE in 1 CARTON / 100 mL in 1 TUBE
Product Details
What is NDC 51230-391?
What are the uses for Noxicare?
Which are Noxicare UNII Codes?
The UNII codes for the active ingredients in this product are:
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y) (Active Moiety)
- TURMERIC (UNII: 856YO1Z64F)
- TURMERIC (UNII: 856YO1Z64F) (Active Moiety)
- OCIMUM TENUIFLORUM TOP (UNII: 34T63W8ULS)
- OCIMUM TENUIFLORUM TOP (UNII: 34T63W8ULS) (Active Moiety)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) (Active Moiety)
- ROSEMARY (UNII: IJ67X351P9)
- ROSEMARY (UNII: IJ67X351P9) (Active Moiety)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- SALIX ALBA BARK (UNII: 205MXS71H7) (Active Moiety)
- GINGER (UNII: C5529G5JPQ)
- GINGER (UNII: C5529G5JPQ) (Active Moiety)
Which are Noxicare 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:
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PETROLATUM (UNII: 4T6H12BN9U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STEARYL STEARATE (UNII: 5WX2EGD0DK)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- WATER (UNII: 059QF0KO0R)
* 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".