NDC 70859-054 Nutriarx Creampak
Triamcinolone Acetonide,Dimethicone Kit Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70859 - Nucare Pharmaceuticals,inc.
- 70859-054 - Nutriarx Creampak
Product Packages
NDC Code 70859-054-01
Package Description: 1 KIT in 1 KIT * 118 mL in 1 BOTTLE (68599-0213-4) * 1 TUBE in 1 CARTON (45802-064-36) / 80 g in 1 TUBE
Product Details
What is NDC 70859-054?
What are the uses for Nutriarx Creampak?
Which are Nutriarx Creampak UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- TRIAMCINOLONE ACETONIDE (UNII: F446C597KA)
- TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (Active Moiety)
Which are Nutriarx Creampak 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- LYSINE (UNII: K3Z4F929H6)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- TYROSINE (UNII: 42HK56048U)
- ARGININE (UNII: 94ZLA3W45F)
- KUKUI NUT OIL (UNII: TP11QR7B8R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TROLAMINE (UNII: 9O3K93S3TK)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PEG-100 STEARATE (UNII: YD01N1999R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- NIACINAMIDE (UNII: 25X51I8RD4)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- OCTENYLSUCCINIC ACID (UNII: 12UZE4X73L)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- LEVOMENOL (UNII: 24WE03BX2T)
- THREONINE (UNII: 2ZD004190S)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ALANINE (UNII: OF5P57N2ZX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GLUTAMIC ACID (UNII: 3KX376GY7L)
- ISOLEUCINE (UNII: 04Y7590D77)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- VALINE (UNII: HG18B9YRS7)
- PHENYLALANINE (UNII: 47E5O17Y3R)
- METHIONINE (UNII: AE28F7PNPL)
- SERINE (UNII: 452VLY9402)
- GLYCINE (UNII: TE7660XO1C)
- ASPARTIC ACID (UNII: 30KYC7MIAI)
- WATER (UNII: 059QF0KO0R)
- GINGER (UNII: C5529G5JPQ)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HISTIDINE (UNII: 4QD397987E)
- CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)
- PROLINE (UNII: 9DLQ4CIU6V)
- LEUCINE (UNII: GMW67QNF9C)
- CYSTEINE (UNII: K848JZ4886)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- CETYL ESTERS WAX (UNII: D072FFP9GU)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- SORBIC ACID (UNII: X045WJ989B)
What is the NDC to RxNorm Crosswalk for Nutriarx Creampak?
- RxCUI: 1014314 - triamcinolone acetonide 0.1 % Topical Cream
- RxCUI: 1014314 - triamcinolone acetonide 1 MG/ML Topical Cream
- RxCUI: 1014314 - triamcinolone acetonide 1 MG per GM Topical Cream
- RxCUI: 259090 - dimethicone 5 % Topical Cream
- RxCUI: 259090 - dimethicone 50 MG/ML Topical Cream
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".