NDC 10596-901 Re/cover Kit
Colloidal Oatmeal Kit Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 10596-901?
What are the uses for Re/cover Kit?
Which are Re/cover Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- OATMEAL (UNII: 8PI54V663Y)
- OATMEAL (UNII: 8PI54V663Y) (Active Moiety)
Which are Re/cover Kit 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PETROLATUM (UNII: 4T6H12BN9U)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- ARGININE (UNII: 94ZLA3W45F)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- LAURETH-3 (UNII: F32E4CB0UJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- ALLANTOIN (UNII: 344S277G0Z)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- PANTHENOL (UNII: WV9CM0O67Z)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
What is the NDC to RxNorm Crosswalk for Re/cover Kit?
- RxCUI: 1545142 - colloidal oatmeal 1 % Topical Ointment
- RxCUI: 1545142 - colloidal oatmeal 0.01 MG/MG Topical Ointment
* 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".