NDC 70859-049 Nudermrxpak 120
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70859 - Nucare Pharmaceuticals,inc.
- 70859-049 - Nudermrxpak 120
Product Packages
NDC Code 70859-049-01
Package Description: 1 KIT in 1 KIT * 118 mL in 1 TUBE (68599-0203-4) * 120 g in 1 TUBE (66993-877-78)
Product Details
What is NDC 70859-049?
What are the uses for Nudermrxpak 120?
Which are Nudermrxpak 120 UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIPOTRIENE (UNII: 143NQ3779B)
- CALCIPOTRIENE (UNII: 143NQ3779B) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Nudermrxpak 120 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:
- DICHLOROBENZYL ALCOHOL (UNII: 1NKX3648J9)
- CETETH-20 (UNII: I835H2IHHX)
- PETROLATUM (UNII: 4T6H12BN9U)
- EDETIC ACID (UNII: 9G34HU7RV0)
- .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- WATER (UNII: 059QF0KO0R)
- MINERAL OIL (UNII: T5L8T28FGP)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PEG-100 STEARATE (UNII: YD01N1999R)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- LEVOMENOL (UNII: 24WE03BX2T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TROLAMINE (UNII: 9O3K93S3TK)
- GINGER (UNII: C5529G5JPQ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- KUKUI NUT OIL (UNII: TP11QR7B8R)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CETYL ALCOHOL (UNII: 936JST6JCN)
What is the NDC to RxNorm Crosswalk for Nudermrxpak 120?
- RxCUI: 259090 - dimethicone 5 % Topical Cream
- RxCUI: 259090 - dimethicone 50 MG/ML Topical Cream
- RxCUI: 313921 - calcipotriene 0.005 % Topical Cream
- RxCUI: 313921 - calcipotriene 0.05 MG/ML Topical Cream
- RxCUI: 313921 - calcipotriene (as calcipotriene monohydrate) 0.005 % Topical Cream
* 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".