NDC 69521-061 Smartpractice Topical Anesthetic Gel Raspberry
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
RED (C48326)
GREEN (C48329)
BUBBLE GUM (C73368)
STRAWBERRY (C73417)
CHERRY (C73375)
MINT (C73404)
RASPBERRY (C73413)
Code Structure Chart
Product Details
What is NDC 69521-061?
What are the uses for Smartpractice Topical Anesthetic Gel Raspberry?
Which are Smartpractice Topical Anesthetic Gel Raspberry 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 Raspberry 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)
- PEPPERMINT (UNII: V95R5KMY2B)
- D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Smartpractice Topical Anesthetic Gel Raspberry?
- 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".