NDC 68400-323 Gelato Topical Anesthetic
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What is NDC 68400-323?
What are the uses for Gelato Topical Anesthetic?
Which are Gelato Topical Anesthetic UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Gelato Topical Anesthetic 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 SODIUM (UNII: SB8ZUX40TY)
What is the NDC to RxNorm Crosswalk for Gelato Topical Anesthetic?
- RxCUI: 1435490 - benzocaine 20 % Oral Spray
- RxCUI: 1435490 - benzocaine 200 MG/ML Oral Spray
- RxCUI: 1435495 - Gelato Anesthetic 20 % Oral Spray
- RxCUI: 1435495 - benzocaine 200 MG/ML Oral Spray [Gelato Anesthetic]
- RxCUI: 1435495 - Gelato Anesthetic 200 MG/ML Oral Spray
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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".