NDC 83220-001 Deluxe Dental Emergency Kit
Epinephrine,Albuterol Sulfate,Nitroglycerin,Diphenhydramine Hydrochloride,Aspirin Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
WHITE (C48325)
RED (C48326 - BLUISH-RED)
10 MM
BAYER
Code Structure Chart
Product Details
What is NDC 83220-001?
What are the uses for Deluxe Dental Emergency Kit?
Which are Deluxe Dental Emergency Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- ALBUTEROL SULFATE (UNII: 021SEF3731)
- ALBUTEROL (UNII: QF8SVZ843E) (Active Moiety)
- NITROGLYCERIN (UNII: G59M7S0WS3)
- NITROGLYCERIN (UNII: G59M7S0WS3) (Active Moiety)
- DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)
- ASPIRIN (UNII: R16CO5Y76E)
- ASPIRIN (UNII: R16CO5Y76E) (Active Moiety)
Which are Deluxe Dental Emergency 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLOROBUTANOL (UNII: HM4YQM8WRC)
- SODIUM BISULFITE (UNII: TZX5469Z6I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ALCOHOL (UNII: 3K9958V90M)
- NORFLURANE (UNII: DH9E53K1Y8)
- OLEIC ACID (UNII: 2UMI9U37CP)
- CALCIUM STEARATE (UNII: 776XM7047L)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- WATER (UNII: 059QF0KO0R)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- STARCH, CORN (UNII: O8232NY3SJ)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- TRIACETIN (UNII: XHX3C3X673)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCERIN (UNII: PDC6A3C0OX)
- HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Deluxe Dental Emergency Kit?
- RxCUI: 1049633 - diphenhydrAMINE HCl 50 MG/ML Injectable Solution
- RxCUI: 1049633 - diphenhydramine hydrochloride 50 MG/ML Injectable Solution
- RxCUI: 1049633 - diphenhydramine HCl 50 MG/ML Injectable Solution
- RxCUI: 1049906 - diphenhydrAMINE HCl 12.5 MG in 5 mL Oral Solution
- RxCUI: 1049906 - diphenhydramine hydrochloride 2.5 MG/ML Oral Solution
* 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.
[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".