NDC 50488-6262 Lidocaine 4%
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What is NDC 50488-6262?
What are the uses for Lidocaine 4%?
Which are Lidocaine 4% UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Lidocaine 4% 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:
- WATER (UNII: 059QF0KO0R)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL 1-STEARATE (UNII: 258491E1RZ)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- ISOSTEARYL PALMITATE (UNII: 9EHU0R7ER1)
- LAURETH-7 (UNII: Z95S6G8201)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Lidocaine 4%?
- RxCUI: 1010895 - lidocaine HCl 4 % Topical Cream
- RxCUI: 1010895 - lidocaine hydrochloride 40 MG/ML Topical Cream
- RxCUI: 1010895 - lidocaine hydrochloride 4 % 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".