NDC 72337-776 Orajel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72337 - Biofilm
- 72337-776 - Orajel
Product Characteristics
Product Packages
NDC Code 72337-776-01
Package Description: 1 PACKAGE in 1 CARTON / 8 g in 1 PACKAGE
Product Details
What is NDC 72337-776?
What are the uses for Orajel?
Which are Orajel UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Orajel 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)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POVIDONE K90 (UNII: RDH86HJV5Z)
- POLYCARBOPHIL (UNII: W25LM17A4W)
- ACID BLUE 9 AMMONIUM (UNII: 86R7G3C26F)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PULLULAN (UNII: 8ZQ0AYU1TT)
- GLYCERIN (UNII: PDC6A3C0OX)
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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".