NDC 68848-001 Topical Anesthetic Anorectal Cream Numb And Number
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68848 - Dermtech Labs Inc. Dba Gd Labs
- 68848-001 - Topical Anesthetic Anorectal Cream
Product Packages
NDC Code 68848-001-02
Package Description: 1 PACKAGE in 1 PACKAGE / 54 g in 1 PACKAGE (68848-001-01)
NDC Code 68848-001-04
Package Description: 1 PACKAGE in 1 PACKAGE / 600 g in 1 PACKAGE (68848-001-03)
Product Details
What is NDC 68848-001?
What are the uses for Topical Anesthetic Anorectal Cream Numb And Number?
Which are Topical Anesthetic Anorectal Cream Numb And Number UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Topical Anesthetic Anorectal Cream Numb And Number 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:
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Topical Anesthetic Anorectal Cream Numb And Number?
- RxCUI: 1366789 - lidocaine 5 % Rectal Cream
- RxCUI: 1366789 - lidocaine 50 MG/ML Rectal Cream
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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".