NDC 52763-504 Lidocream 5
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52763 - Golden Touch Llc
- 52763-504 - Lidocream 5
Product Packages
NDC Code 52763-504-80
Package Description: 480 g in 1 JAR
Product Details
What is NDC 52763-504?
What are the uses for Lidocream 5?
Which are Lidocream 5 UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Lidocream 5 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- ALCOHOL (UNII: 3K9958V90M)
- SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Lidocream 5?
- RxCUI: 1534792 - lidocaine 5 % Topical Cream
- RxCUI: 1534792 - lidocaine 50 MG/ML Topical Cream
- RxCUI: 1544065 - LidoCream5 5 % Topical Cream
- RxCUI: 1544065 - lidocaine 50 MG/ML Topical Cream [Lidocream]
- RxCUI: 1544065 - Lidocream 5 % Topical Cream
* Please review the disclaimer below.
[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".