NDC 55628-9047 Ultracin T
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55628 - Cal Pharma
- 55628-9047 - Ultracin T
Product Packages
NDC Code 55628-9047-4
Package Description: 120 mL in 1 TUBE
Product Details
What is NDC 55628-9047?
What are the uses for Ultracin T?
Which are Ultracin T UNII Codes?
The UNII codes for the active ingredients in this product are:
- TROLAMINE SALICYLATE (UNII: H8O4040BHD)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Ultracin T 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:
- (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- BOSWELLIA SERRATA WHOLE (UNII: X7B7P649WQ)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GAULTHERIA PROCUMBENS LEAF (UNII: 2125M16OWN)
- GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PETASITES HYBRIDUS LEAF (UNII: JOS311ZC1G)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MARITIME PINE (UNII: 50JZ5Z98QY)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WILLOW BARK (UNII: S883J9JDYX)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- WATER (UNII: 059QF0KO0R)
- ZANTHOXYLUM AMERICANUM BARK (UNII: A4KL1HMZ7T)
- ZINGIBER OFFICINALE WHOLE (UNII: IN6Q3S3414)
What is the NDC to RxNorm Crosswalk for Ultracin T?
- 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".