NDC 51230-418 Tru-micin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 51230-418?
What are the uses for Tru-micin?
Which are Tru-micin UNII Codes?
The UNII codes for the active ingredients in this product are:
- TROLAMINE (UNII: 9O3K93S3TK)
- TROLAMINE (UNII: 9O3K93S3TK) (Active Moiety)
Which are Tru-micin 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- COCO-CAPRYLATE (UNII: 4828G836N6)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL STEARATE (UNII: 5WX2EGD0DK)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PETROLATUM (UNII: 4T6H12BN9U)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- WATER (UNII: 059QF0KO0R)
- TURMERIC (UNII: 856YO1Z64F)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- OCIMUM TENUIFLORUM TOP (UNII: 34T63W8ULS)
- GINGER (UNII: C5529G5JPQ)
- ROSEMARY (UNII: IJ67X351P9)
What is the NDC to RxNorm Crosswalk for Tru-micin?
- RxCUI: 1433915 - Tru-micin 10 % Topical Lotion
- RxCUI: 1433915 - trolamine salicylate 100 MG/ML Topical Lotion [Tru-micin]
- RxCUI: 1433915 - Tru-micin 100 MG/ML Topical Lotion
- RxCUI: 313519 - trolamine salicylate 10 % Topical Lotion
- RxCUI: 313519 - trolamine salicylate 100 MG/ML Topical Lotion
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[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".