NDC 67334-0457 T.r.u.e. Test Thin-layer Rapid Use Patch Test
Standardized Allergenic Kit Cutaneous - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67334 - Smartpractice Denmark Aps
- 67334-0457 - T.r.u.e. Test
Product Packages
NDC Code 67334-0457-1
Package Description: 5 CELLO PACK in 1 BOX / 1 KIT in 1 CELLO PACK * 1 PATCH in 1 POUCH / 48 h in 1 PATCH * 1 PATCH in 1 POUCH / 48 h in 1 PATCH * 1 PATCH in 1 POUCH / 48 h in 1 PATCH
Product Details
What is NDC 67334-0457?
What are the uses for T.r.u.e. Test Thin-layer Rapid Use Patch Test?
Which are T.r.u.e. Test Thin-layer Rapid Use Patch Test UNII Codes?
The UNII codes for the active ingredients in this product are:
- NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68)
- NICKEL CATION (UNII: OIS2CXW7AM) (Active Moiety)
- LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
- LANOLIN ALCOHOLS (UNII: 884C3FA9HE) (Active Moiety)
- NEOMYCIN SULFATE (UNII: 057Y626693)
- NEOMYCIN (UNII: I16QD7X297) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
- TETRACAINE HYDROCHLORIDE (UNII: 5NF5D4OPCI)
- TETRACAINE (UNII: 0619F35CGV) (Active Moiety)
- DIBUCAINE HYDROCHLORIDE (UNII: Z97702A5DG)
- DIBUCAINE (UNII: L6JW2TJG99) (Active Moiety)
- GERANIOL (UNII: L837108USY)
- GERANIOL (UNII: L837108USY) (Active Moiety)
- CINNAMALDEHYDE (UNII: SR60A3XG0F)
- CINNAMALDEHYDE (UNII: SR60A3XG0F) (Active Moiety)
- CINNAMYL ALCOHOL (UNII: SS8YOP444F)
- CINNAMYL ALCOHOL (UNII: SS8YOP444F) (Active Moiety)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR) (Active Moiety)
- EUGENOL (UNII: 3T8H1794QW)
- EUGENOL (UNII: 3T8H1794QW) (Active Moiety)
- ISOEUGENOL (UNII: 5M0MWY797U)
- ISOEUGENOL (UNII: 5M0MWY797U) (Active Moiety)
- .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
- .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418) (Active Moiety)
- EVERNIA PRUNASTRI (UNII: O3034Q5AHK)
- EVERNIA PRUNASTRI (UNII: O3034Q5AHK) (Active Moiety)
- ROSIN (UNII: 88S87KL877)
- ROSIN (UNII: 88S87KL877) (Active Moiety)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PROPYLPARABEN (UNII: Z8IX2SC1OH) (Active Moiety)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- METHYLPARABEN (UNII: A2I8C7HI9T) (Active Moiety)
- ETHYLPARABEN (UNII: 14255EXE39)
- ETHYLPARABEN (UNII: 14255EXE39) (Active Moiety)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- BUTYLPARABEN (UNII: 3QPI1U3FV8) (Active Moiety)
- BENZYLPARABEN (UNII: 8Y41DYV4VG)
- BENZYLPARABEN (UNII: 8Y41DYV4VG) (Active Moiety)
- BALSAM PERU (UNII: 8P5F881OCY)
- BALSAM PERU (UNII: 8P5F881OCY) (Active Moiety)
- ETHYLENEDIAMINE (UNII: 60V9STC53F)
- ETHYLENEDIAMINE (UNII: 60V9STC53F) (Active Moiety)
- COBALTOUS CHLORIDE HEXAHYDRATE (UNII: 17AVG63ZBC)
- COBALTOUS CATION (UNII: AI1MR454XG) (Active Moiety)
- P-TERT-BUTYLPHENOL-FORMALDEHYDE RESIN (LOW MOLECULAR WEIGHT) (UNII: Q51LPW21CH)
- P-TERT-BUTYLPHENOL-FORMALDEHYDE RESIN (LOW MOLECULAR WEIGHT) (UNII: Q51LPW21CH) (Active Moiety)
- BISPHENOL A DIGLYCIDYL ETHER (UNII: F3XRM1NX4H)
- BISPHENOL A DIGLYCIDYL ETHER (UNII: F3XRM1NX4H) (Active Moiety)
- DIPHENYLGUANIDINE (UNII: 6MRZ85RNHQ)
- DIPHENYLGUANIDINE (UNII: 6MRZ85RNHQ) (Active Moiety)
- DITIOCARB ZINC (UNII: ICW4708Z8G)
- DITIOCARB ZINC (UNII: ICW4708Z8G) (Active Moiety)
- ZINC DIBUTYLDITHIOCARBAMATE (UNII: HNM5J934VP)
- ZINC DIBUTYLDITHIOCARBAMATE (UNII: HNM5J934VP) (Active Moiety)
- N-ISOPROPYL-N'-PHENYL-1,4-PHENYLENEDIAMINE (UNII: 0M7PSL4100)
- N-ISOPROPYL-N'-PHENYL-1,4-PHENYLENEDIAMINE (UNII: 0M7PSL4100) (Active Moiety)
- N-CYCLOHEXYL-N'-PHENYL-P-PHENYLENEDIAMINE (UNII: T29JGK5V4R)
- N-CYCLOHEXYL-N'-PHENYL-P-PHENYLENEDIAMINE (UNII: T29JGK5V4R) (Active Moiety)
- N,N'-DIPHENYL-P-PHENYLENEDIAMINE (UNII: DD517SCM92)
- N,N'-DIPHENYL-P-PHENYLENEDIAMINE (UNII: DD517SCM92) (Active Moiety)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) (Active Moiety)
- QUATERNIUM-15 (UNII: E40U03LEM0)
- QUATERNIUM-15 (UNII: E40U03LEM0) (Active Moiety)
- METHYLDIBROMO GLUTARONITRILE (UNII: YX089CPS05)
- METHYLDIBROMO GLUTARONITRILE (UNII: YX089CPS05) (Active Moiety)
- P-PHENYLENEDIAMINE (UNII: U770QIT64J)
- P-PHENYLENEDIAMINE (UNII: U770QIT64J) (Active Moiety)
- FORMALDEHYDE (UNII: 1HG84L3525)
- FORMALDEHYDE (UNII: 1HG84L3525) (Active Moiety)
- N-CYCLOHEXYL-2-BENZOTHIAZOSULFENAMIDE (UNII: UCA53G94EV)
- N-CYCLOHEXYL-2-BENZOTHIAZOSULFENAMIDE (UNII: UCA53G94EV) (Active Moiety)
- 2,2'-DITHIOBISBENZOTHIAZOLE (UNII: 6OK753033Z)
- 2,2'-DITHIOBISBENZOTHIAZOLE (UNII: 6OK753033Z) (Active Moiety)
- MORPHOLINYLMERCAPTOBENZOTHIAZOLE (UNII: VCD7623F3K)
- MORPHOLINYLMERCAPTOBENZOTHIAZOLE (UNII: VCD7623F3K) (Active Moiety)
- THIMEROSAL (UNII: 2225PI3MOV)
- ETHYLMERCURITHIOSALICYLIC ACID (UNII: 4071N4J64W) (Active Moiety)
- TETRAMETHYLTHIURAM MONOSULFIDE (UNII: 01W430XXSQ)
- TETRAMETHYLTHIURAM MONOSULFIDE (UNII: 01W430XXSQ) (Active Moiety)
- THIRAM (UNII: 0D771IS0FH)
- THIRAM (UNII: 0D771IS0FH) (Active Moiety)
- DISULFIRAM (UNII: TR3MLJ1UAI)
- DISULFIRAM (UNII: TR3MLJ1UAI) (Active Moiety)
- DIPENTAMETHYLENETHIURAM DISULFIDE (UNII: CR113982E5)
- DIPENTAMETHYLENETHIURAM DISULFIDE (UNII: CR113982E5) (Active Moiety)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) (Active Moiety)
- CLIOQUINOL (UNII: 7BHQ856EJ5)
- CLIOQUINOL (UNII: 7BHQ856EJ5) (Active Moiety)
- CHLORQUINALDOL (UNII: D6VHC87LLS)
- CHLORQUINALDOL (UNII: D6VHC87LLS) (Active Moiety)
- TIXOCORTOL PIVALATE (UNII: 6K28E35M3B)
- TIXOCORTOL (UNII: ZX3KEK657Z) (Active Moiety)
- GOLD SODIUM THIOSULFATE (UNII: CKS1YQ9W1J)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- IMIDUREA (UNII: M629807ATL)
- IMIDUREA (UNII: M629807ATL) (Active Moiety)
- BUDESONIDE (UNII: Q3OKS62Q6X)
- BUDESONIDE (UNII: Q3OKS62Q6X) (Active Moiety)
- HYDROCORTISONE BUTYRATE (UNII: 05RMF7YPWN)
- HYDROCORTISONE (UNII: WI4X0X7BPJ) (Active Moiety)
- 2-MERCAPTOBENZOTHIAZOLE (UNII: 5RLR54Z22K)
- 2-MERCAPTOBENZOTHIAZOLE (UNII: 5RLR54Z22K) (Active Moiety)
- BACITRACIN (UNII: 58H6RWO52I)
- BACITRACIN (UNII: 58H6RWO52I) (Active Moiety)
- PARTHENOLIDE (UNII: 2RDB26I5ZB)
- PARTHENOLIDE (UNII: 2RDB26I5ZB) (Active Moiety)
- DISPERSE BLUE 106 (UNII: C48O4QYD6N)
- DISPERSE BLUE 106 (UNII: C48O4QYD6N) (Active Moiety)
- BRONOPOL (UNII: 6PU1E16C9W)
- BRONOPOL (UNII: 6PU1E16C9W) (Active Moiety)
Which are T.r.u.e. Test Thin-layer Rapid Use Patch Test 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:
- HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- BETADEX (UNII: JV039JZZ3A)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM CARBONATE (UNII: 45P3261C7T)
* 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.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[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".