NDC 70859-057 Nusurgepak Surgical Prep/carepak
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70859 - Nucare Pharmaceuticals Inc
- 70859-057 - Nusurgepak Surgical Prep/carepak
Product Packages
NDC Code 70859-057-01
Package Description: 1 KIT in 1 KIT * 118 mg in 1 BOTTLE (68599-0213-4) * 237 mL in 1 BOTTLE, PLASTIC (0116-1061-08) * 22 g in 1 TUBE (68462-180-22)
Product Details
What is NDC 70859-057?
What are the uses for Nusurgepak Surgical Prep/carepak?
Which are Nusurgepak Surgical Prep/carepak UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
- CHLORHEXIDINE (UNII: R4KO0DY52L) (Active Moiety)
- MUPIROCIN (UNII: D0GX863OA5)
- MUPIROCIN (UNII: D0GX863OA5) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Nusurgepak Surgical Prep/carepak 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:
- HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- WATER (UNII: 059QF0KO0R)
- TRIDECYL ALCOHOL (UNII: 8I9428H868)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- PEG-75 LANOLIN (UNII: 09179OX7TB)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- ISOLEUCINE (UNII: 04Y7590D77)
- TROLAMINE (UNII: 9O3K93S3TK)
- OCTENYLSUCCINIC ACID (UNII: 12UZE4X73L)
- GLUTAMIC ACID (UNII: 3KX376GY7L)
- SERINE (UNII: 452VLY9402)
- KUKUI NUT OIL (UNII: TP11QR7B8R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALANINE (UNII: OF5P57N2ZX)
- GLYCINE (UNII: TE7660XO1C)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- LYSINE (UNII: K3Z4F929H6)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- NIACINAMIDE (UNII: 25X51I8RD4)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- LEVOMENOL (UNII: 24WE03BX2T)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- ARGININE (UNII: 94ZLA3W45F)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- ASPARTIC ACID (UNII: 30KYC7MIAI)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- VALINE (UNII: HG18B9YRS7)
- GINGER (UNII: C5529G5JPQ)
- HISTIDINE (UNII: 4QD397987E)
- PROLINE (UNII: 9DLQ4CIU6V)
- LEUCINE (UNII: GMW67QNF9C)
- CYSTEINE (UNII: K848JZ4886)
- METHIONINE (UNII: AE28F7PNPL)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PHENYLALANINE (UNII: 47E5O17Y3R)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- TYROSINE (UNII: 42HK56048U)
- THREONINE (UNII: 2ZD004190S)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
What is the NDC to RxNorm Crosswalk for Nusurgepak Surgical Prep/carepak?
- RxCUI: 106346 - mupirocin 2 % Topical Ointment
- RxCUI: 106346 - mupirocin 0.02 MG/MG Topical Ointment
- RxCUI: 106346 - mupirocin 20 MG per GM Topical Ointment
- RxCUI: 211365 - chlorhexidine gluconate 4 % Medicated Liquid Soap
- RxCUI: 211365 - chlorhexidine gluconate 40 MG/ML Medicated Liquid Soap
* 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".