NDC 58133-650 Radx
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 58133-650?
What are the uses for Radx?
Which are Radx UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Radx 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:
- .ALPHA.-TOCOPHEROL LINOLEATE, D- (UNII: G0N132Q0ED)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SILK, ACID HYDROLYZED (1000 MW) (UNII: 8549W658QV)
- ALLANTOIN (UNII: 344S277G0Z)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- PAPAYA (UNII: KU94FIY6JB)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ETHYLHEXYL OLEATE (UNII: R34927QY59)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- CETYL PHOSPHATE (UNII: VT07D6X67O)
- COCONUT OIL (UNII: Q9L0O73W7L)
- HIPPOPHAE RHAMNOIDES FRUIT OIL (UNII: TA4JCF9S1J)
- HYDROGENATED OLIVE OIL UNSAPONIFIABLES (UNII: B8MIX97W95)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- SODIUM CARBOXYMETHYL .BETA.-GLUCAN (DS 0.65-0.85) (UNII: 2YGO1190AP)
- FRUIT BROMELAIN (UNII: F0ZCA6O9QT)
- WATER (UNII: 059QF0KO0R)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
What is the NDC to RxNorm Crosswalk for Radx?
- RxCUI: 2565921 - lidocaine 2 % Topical Lotion
- RxCUI: 2565921 - lidocaine 20 MG/ML Topical Lotion
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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".