NDC 54879-005 Triacin-c
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54879 - Sti Pharma Llc
- 54879-005 - Triacin-c
Product Characteristics
Product Packages
NDC Code 54879-005-16
Package Description: 473 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54879-005?
Which are Triacin-c UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRIPROLIDINE HYDROCHLORIDE (UNII: YAN7R5L890)
- TRIPROLIDINE (UNII: 2L8T9S52QM) (Active Moiety)
- PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N)
- PSEUDOEPHEDRINE (UNII: 7CUC9DDI9F) (Active Moiety)
- CODEINE PHOSPHATE (UNII: GSL05Y1MN6)
- CODEINE ANHYDROUS (UNII: UX6OWY2V7J) (Active Moiety)
Which are Triacin-c 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:
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ALCOHOL (UNII: 3K9958V90M)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SORBITOL (UNII: 506T60A25R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- CARAMEL (UNII: T9D99G2B1R)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Triacin-c?
- RxCUI: 996640 - codeine phosphate 2 MG/ML / pseudoephedrine hydrochloride 6 MG/ML / triprolidine hydrochloride 0.25 MG/ML Oral Solution
- RxCUI: 996640 - codeine phosphate 10 MG / pseudoephedrine HCl 30 MG / triprolidine HCl 1.25 MG per 5 ML Oral Solution
- RxCUI: 996650 - codeine phosphate 2 MG/ML / pseudoephedrine hydrochloride 6 MG/ML / triprolidine hydrochloride 0.25 MG/ML Oral Solution [Triacin C]
- RxCUI: 996650 - Triacin C (codeine phosphate 10 MG / pseudoephedrine HCl 30 MG / triprolidine HCl 1.25 MG) per 5 ML Oral Solution
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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".