NDC 63742-110 Quick Numb
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63742 - Clinical Resolution Laboratory, Inc.
- 63742-110 - Quick Numb
Product Packages
NDC Code 63742-110-01
Package Description: 35.43 g in 1 BOTTLE
Product Details
What is NDC 63742-110?
What are the uses for Quick Numb?
Which are Quick Numb UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Quick Numb 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:
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- HYDROGENATED POLYDECENE (1500 CST) (UNII: 4YI0729529)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Quick Numb?
- RxCUI: 1534792 - lidocaine 5 % Topical Cream
- RxCUI: 1534792 - lidocaine 50 MG/ML Topical 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".