NDC 67659-400 Dentek Eugenol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67659 - Team Technologies, Inc
- 67659-400 - Dentek Eugenol
Product Characteristics
Product Packages
NDC Code 67659-400-21
Package Description: 1 VIAL, GLASS in 1 KIT / 3.5 mL in 1 VIAL, GLASS (67659-400-20)
Product Details
What is NDC 67659-400?
What are the uses for Dentek Eugenol?
Which are Dentek Eugenol UNII Codes?
The UNII codes for the active ingredients in this product are:
- EUGENOL (UNII: 3T8H1794QW)
- EUGENOL (UNII: 3T8H1794QW) (Active Moiety)
Which are Dentek Eugenol 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:
- SESAME OIL (UNII: QX10HYY4QV)
What is the NDC to RxNorm Crosswalk for Dentek Eugenol?
- RxCUI: 244327 - eugenol 85 % Dental Solution
- RxCUI: 244327 - eugenol 850 MG/ML Topical Solution
- RxCUI: 244327 - eugenol 85 % Topical Solution
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[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".