NDC 75834-101 Psoriatar (coal Tar)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75834 - Nivagen Pharmaceuticals, Inc.
- 75834-101 - Psoriatar (coal Tar)
Product Packages
NDC Code 75834-101-01
Package Description: 1 CAN in 1 CARTON / 100 g in 1 CAN
Product Details
What is NDC 75834-101?
What are the uses for Psoriatar (coal Tar)?
Which are Psoriatar (coal Tar) UNII Codes?
The UNII codes for the active ingredients in this product are:
- COAL TAR (UNII: R533ESO2EC)
- COAL TAR (UNII: R533ESO2EC) (Active Moiety)
Which are Psoriatar (coal Tar) 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:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- ISOBUTANE (UNII: BXR49TP611)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPANE (UNII: T75W9911L6)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Psoriatar (coal Tar)?
- RxCUI: 824335 - crude coal tar 2 % Topical Foam
- RxCUI: 824335 - coal tar 20 MG/ML Topical Foam
- RxCUI: 824335 - coal tar 2 % Topical Foam
- RxCUI: 824335 - crude coal tar 2 % (coal tar solution 10 % ) Topical Foam
* 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".