NDC 70859-043 Medicated Buccal Dna Collection Kit
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70859 - Nucare Pharmaceuticals,inc.
- 70859-043 - Medicated Buccal Dna Collection Kit
Product Packages
NDC Code 70859-043-01
Package Description: 1 KIT in 1 PACKAGE * 15 mL in 1 CUP, UNIT-DOSE (50383-775-15)
Product Details
What is NDC 70859-043?
What are the uses for Medicated Buccal Dna Collection Kit?
Which are Medicated Buccal Dna Collection Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE ANHYDROUS (UNII: EC2CNF7XFP)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Medicated Buccal Dna Collection 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:
- ORANGE (UNII: 5EVU04N5QU)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN (UNII: FST467XS7D)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for Medicated Buccal Dna Collection Kit?
- RxCUI: 1010739 - lidocaine HCl 2 % Mucous Membrane Topical Solution
- RxCUI: 1010739 - lidocaine hydrochloride 20 MG/ML Mucous Membrane Topical Solution
- RxCUI: 1010739 - lidocaine HCl 2 % Oral Topical Solution
- RxCUI: 1010739 - lidocaine HCl 2 % Oromucosal Solution
* 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".