NDC 69521-021 Smartpractice Topical Anesthetic Gel Cherry
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69521 - Smarthealth, Inc. (dba Smartpractice)
- 69521-021 - Smartpractice Topical Anesthetic Gel
Product Characteristics
RED (C48326)
BUBBLE GUM (C73368)
STRAWBERRY (C73417)
CHERRY (C73375)
Product Packages
NDC Code 69521-021-34
Package Description: 34 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 69521-021?
What are the uses for Smartpractice Topical Anesthetic Gel Cherry?
Which are Smartpractice Topical Anesthetic Gel Cherry UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Smartpractice Topical Anesthetic Gel Cherry 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:
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SACCHARIN (UNII: FST467XS7D)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- WATER (UNII: 059QF0KO0R)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Smartpractice Topical Anesthetic Gel Cherry?
- RxCUI: 238910 - benzocaine 20 % Oral Gel
- RxCUI: 238910 - benzocaine 0.2 MG/MG Oral Gel
- RxCUI: 238910 - benzocaine 20 % (180-220 MG per 1 GM) Oral Gel
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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".